An established, full-service agency is looking for an Account Manager to join their brilliant team in Berkshire. With broad expertise across medical education, brand marketing and multichannel campaigns, this dynamic, independent agency enjoys strong client relationships and has several exciting new projects in the works. This is a fantastic opportunity for an individual looking for exposure, variety and growth. As AM you'll manage day to day project delivery across an interesting mix of accounts and deliverables. You'll be a point of contact for clients, liaise with writers and creatives, and ensure work is completed on time and on budget. This mid-size agency has a sociable and collaborative culture; you'll be joining an ambitious team who are passionate about working on meaningful campaigns that make a difference in healthcare. You'll enjoy opportunities to further your skills and plenty of support to help you progress. Requirements To be considered for this position you'll need a healthcare communications agency background to SAE/AM level, strong project management and people skills, and a drive to deliver great work. You will be self-motivated, enthusiastic, and comfortable in a fast-paced agency setting.
Jun 27, 2025
Full time
An established, full-service agency is looking for an Account Manager to join their brilliant team in Berkshire. With broad expertise across medical education, brand marketing and multichannel campaigns, this dynamic, independent agency enjoys strong client relationships and has several exciting new projects in the works. This is a fantastic opportunity for an individual looking for exposure, variety and growth. As AM you'll manage day to day project delivery across an interesting mix of accounts and deliverables. You'll be a point of contact for clients, liaise with writers and creatives, and ensure work is completed on time and on budget. This mid-size agency has a sociable and collaborative culture; you'll be joining an ambitious team who are passionate about working on meaningful campaigns that make a difference in healthcare. You'll enjoy opportunities to further your skills and plenty of support to help you progress. Requirements To be considered for this position you'll need a healthcare communications agency background to SAE/AM level, strong project management and people skills, and a drive to deliver great work. You will be self-motivated, enthusiastic, and comfortable in a fast-paced agency setting.
Are you a seasoned healthcare advertising expert read to shape the future of an ambitious, creatively driven agency? This is a rare opportunity to join a boutique but scaling team. They're looking for a Group Account Director to help evolve their offering and take the lead on global creative campaigns across pharma and biotech clients. What you'll be doing: Leading strategic direction on global pharmaceutical campaigns Writing creative briefs and working closely with creatives to shape standout work Supporting new business efforts through pitching and networking Taking a hands-on role in delivery while guiding and mentoring a growing team What you'll bring: Extensive experience in health/medical advertising and brand agencies A strong track record of in brand leadership and digital first campaign strategy Experience working across global markets and complex client needs Confidence in pitching, leading teams, and translating strategy into creative output Previous agency experience in healthcare advertising or consulting firm What's on offer: Hybrid working 2 days in the office Competitive salary Access to global tools, support and innovation platforms through agency network The opportunity to build and shape the team and agency If you're looking to play a key role in the next phase of a growing creative agency's evolution- apply now! For more information please contact Nicky Stunt at for more info.
Jun 25, 2025
Full time
Are you a seasoned healthcare advertising expert read to shape the future of an ambitious, creatively driven agency? This is a rare opportunity to join a boutique but scaling team. They're looking for a Group Account Director to help evolve their offering and take the lead on global creative campaigns across pharma and biotech clients. What you'll be doing: Leading strategic direction on global pharmaceutical campaigns Writing creative briefs and working closely with creatives to shape standout work Supporting new business efforts through pitching and networking Taking a hands-on role in delivery while guiding and mentoring a growing team What you'll bring: Extensive experience in health/medical advertising and brand agencies A strong track record of in brand leadership and digital first campaign strategy Experience working across global markets and complex client needs Confidence in pitching, leading teams, and translating strategy into creative output Previous agency experience in healthcare advertising or consulting firm What's on offer: Hybrid working 2 days in the office Competitive salary Access to global tools, support and innovation platforms through agency network The opportunity to build and shape the team and agency If you're looking to play a key role in the next phase of a growing creative agency's evolution- apply now! For more information please contact Nicky Stunt at for more info.
QA Manager I am partnered with an international advanced pharmaceutical and medical device business that are investing seriously into expanding their quality and operational activities, especially across various sites within the UK. After the appointment of a new senior quality leadership team, the business is now looking to bring in new management across critical sites. Working as a form of QA head for their own respective site, this position will manage a small team and remain fully hands on in all areas of quality. This includes systems oversight, operational delivery and validation activities. A core aspect of the role will be leadership leading a small team through hands on coaching, mentoring and training. If you are looking for a varied position that offers you a chance to make a real impact on your own site and play a significant part in the way that quality assurance is adopted and implemented business wide, please apply below or contact Mark Bux-Ryan for further information. Key experience: Experienced within a QA capacity, working in a GMP environment Ideally working experience of a sterile / aseptic environment working within a terminally sterile setting would be helpful these are not essential Leadership and management experience is preferred Strong hands on experience of a range of quality activities, especially in relation to QMS oversight Auditing experience essential if you have been a lead auditor, this would be advantageous Knowledge and experience of validation activities Quality, assurance, qa, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, specialist, compliance, regulatory, audit, lead, complaints
Jun 20, 2025
Full time
QA Manager I am partnered with an international advanced pharmaceutical and medical device business that are investing seriously into expanding their quality and operational activities, especially across various sites within the UK. After the appointment of a new senior quality leadership team, the business is now looking to bring in new management across critical sites. Working as a form of QA head for their own respective site, this position will manage a small team and remain fully hands on in all areas of quality. This includes systems oversight, operational delivery and validation activities. A core aspect of the role will be leadership leading a small team through hands on coaching, mentoring and training. If you are looking for a varied position that offers you a chance to make a real impact on your own site and play a significant part in the way that quality assurance is adopted and implemented business wide, please apply below or contact Mark Bux-Ryan for further information. Key experience: Experienced within a QA capacity, working in a GMP environment Ideally working experience of a sterile / aseptic environment working within a terminally sterile setting would be helpful these are not essential Leadership and management experience is preferred Strong hands on experience of a range of quality activities, especially in relation to QMS oversight Auditing experience essential if you have been a lead auditor, this would be advantageous Knowledge and experience of validation activities Quality, assurance, qa, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, specialist, compliance, regulatory, audit, lead, complaints
My Client, who are a software company based in the financial industry are looking for an experienced Systems Administrator with a strong background working with Linux to be the point of contact for Linux based issues and lead Linux projects. You will be expected to provide support to colleagues within the business and work on pre planned projects in order to keep the infrastructure, software and hardware up to date and secure. You will be joining an innovative and growing team with plenty of opportunity to further your career and develop your knowledge. Main Responsibilities: Must be highly experienced and confident with Linux Administration. The successful candidate will be able to work as a member of a team of Systems Administrators performing a variety of tasks from performing daily system checks to delivery of new business projects and applications. Managing, maintaining and securing of internal IT infrastructure. This includes, Servers, Hardware, Virtual Environment, LAN & WAN, Storage and Telecoms. Implementation of new technology as part of many upcoming projects. Providing escalation support to the other internal IT teams. Other Duties and Responsibilities: Maintaining up to date and effective documentation on all relevant IT systems, services and procedures. Assisting in the Development and control of the IT security policy and associated policies. Ensuring security on all systems and legal requirements are met. Assisting in the management and responsibility for company data ensuring that all backup and restore procedures are adhered to and effective. Ensuring that any planned changes to the IT infrastructure are efficient, viable and documented in line with Change Control methodologies. Provision, configure, and manage new systems and software. Ensure service availability is monitored and that appropriate alerts are set up. Provide infrastructure support for our hosting environments and Intranet, including managing code deployments, software configuration, performance monitoring, troubleshooting, patch management, end-user coordination, and other day-to-day support. Candidate Requirements (You do not need to have experience in all of these areas, but the more the better): Linux Systems Administrator with at least 5 years of experience Experience working in a CentOS and/or RedHat environment Physical and virtual Servers (VMware, OnApp or XenServer) Installing, configuring, and administering Linux operating systems Experience with open-source software and/or service management tools and applications Knowledge of monitoring solutions (Zabbix/Nagios/Graylog/Grafana) Scripting languages such as Bash, PHP, Perl, and/or Python Good understanding of server security issues and best practices for security software policies Practical knowledge of building and supporting physical server components and RAID Previous experience working in an environment with formally structured IT Operational processes: work request ticket management, incident management, change management, problem management Experience with Hardware/Software migration Demonstrates a strongly detail-oriented approach to everything you do Can adapt to change and work well under pressure Ability to take on internal operational initiatives as a prime or lead Excellent communication, organisational, interpersonal, problem solving, and documentation skills Working knowledge of local and wide area networking and associated technologies, eg Switches, Routers, Firewalls, VPN's, etc. Any experience working within a Microsoft environment would be useful, but not a deal breaker if you don't. Pro-active, collaborative team member Keen to continuously develop knowledge of different technologies
Dec 14, 2022
Full time
My Client, who are a software company based in the financial industry are looking for an experienced Systems Administrator with a strong background working with Linux to be the point of contact for Linux based issues and lead Linux projects. You will be expected to provide support to colleagues within the business and work on pre planned projects in order to keep the infrastructure, software and hardware up to date and secure. You will be joining an innovative and growing team with plenty of opportunity to further your career and develop your knowledge. Main Responsibilities: Must be highly experienced and confident with Linux Administration. The successful candidate will be able to work as a member of a team of Systems Administrators performing a variety of tasks from performing daily system checks to delivery of new business projects and applications. Managing, maintaining and securing of internal IT infrastructure. This includes, Servers, Hardware, Virtual Environment, LAN & WAN, Storage and Telecoms. Implementation of new technology as part of many upcoming projects. Providing escalation support to the other internal IT teams. Other Duties and Responsibilities: Maintaining up to date and effective documentation on all relevant IT systems, services and procedures. Assisting in the Development and control of the IT security policy and associated policies. Ensuring security on all systems and legal requirements are met. Assisting in the management and responsibility for company data ensuring that all backup and restore procedures are adhered to and effective. Ensuring that any planned changes to the IT infrastructure are efficient, viable and documented in line with Change Control methodologies. Provision, configure, and manage new systems and software. Ensure service availability is monitored and that appropriate alerts are set up. Provide infrastructure support for our hosting environments and Intranet, including managing code deployments, software configuration, performance monitoring, troubleshooting, patch management, end-user coordination, and other day-to-day support. Candidate Requirements (You do not need to have experience in all of these areas, but the more the better): Linux Systems Administrator with at least 5 years of experience Experience working in a CentOS and/or RedHat environment Physical and virtual Servers (VMware, OnApp or XenServer) Installing, configuring, and administering Linux operating systems Experience with open-source software and/or service management tools and applications Knowledge of monitoring solutions (Zabbix/Nagios/Graylog/Grafana) Scripting languages such as Bash, PHP, Perl, and/or Python Good understanding of server security issues and best practices for security software policies Practical knowledge of building and supporting physical server components and RAID Previous experience working in an environment with formally structured IT Operational processes: work request ticket management, incident management, change management, problem management Experience with Hardware/Software migration Demonstrates a strongly detail-oriented approach to everything you do Can adapt to change and work well under pressure Ability to take on internal operational initiatives as a prime or lead Excellent communication, organisational, interpersonal, problem solving, and documentation skills Working knowledge of local and wide area networking and associated technologies, eg Switches, Routers, Firewalls, VPN's, etc. Any experience working within a Microsoft environment would be useful, but not a deal breaker if you don't. Pro-active, collaborative team member Keen to continuously develop knowledge of different technologies
RBW are collaborating with a leading international biotech to find an Associate Director of Regulatory Affairs Strategy, who will participate in the development and implementation of regulatory strategy for a range of therapeutic areas, including Pulmonology/Respiratory, Haematology, Diabetes and Gene therapies. The role is based in their international HQ in London. Role Responsibilities: Act as the Regional Regulatory Lead, to develop regulatory strategy for assigned products in collaboration with Global Regulatory Lead Ensure projects are appropriately prioritised and progressed in accordance with agreed regulatory plans, communicating any identified risks to project teams and Senior Management Manage the preparation and submission of technically complex regulatory submissions, with minimal supervision Provide appropriate strategic regulatory advice to Submission and Project Teams in a timely manner Keep regulatory affairs senior management informed on the status of global strategies and tactics, procedures and practices, with a focus on regulatory and policy trends in the EU Act as primary contact with Regulatory Authorities for assigned products and territories Lead local or global company process improvement initiatives Ensure all work is compliant with regulatory requirements and company policies and procedures Work with cross-department teams and key IHQ functions to achieve corporate and departmental goals and objectives. Able to plan, schedule and arrange own work activities with limited direction, exhibiting ownership and accountability for all projects and internal assignments Role Requirements: Bachelor s degree in life sciences Recent direct experience of clinical development Has led direct interactions with EMA, and national Competent Authorities on clinical development and complex regulatory submissions such as MAAs, new indications, and PIPs In-depth knowledge of regulatory landscape, including ICH and regional requirements for assigned territories and current regulatory trends Recognized as a knowledgeable resource for regulatory advice in other departments Desire to be part of a highly innovative company aimed at transforming the lives of people with serious diseases, their families and society Display solid ethics and fully comply with all regulatory, legal and industry codes of conduct Strategic ability, as evidenced by an awareness of the "big picture" strategic issues facing the business overall and positioning of local strategy relative to global and international requirements Ability to navigate and be successful in a fast-paced environment while delivering high quality results Adaptable to changing plans and able to behave independently with minimal guidance where needed, but also embraces being part of a team and working collaboratively Good interpersonal skills and ability to deal effectively with a variety of personalities Acts to promote an energizing, inclusive environment and good morale Empowers other team members through delegation of tasks and decisions Excellent communication skills, strong oral/written presentation skills. Fluent written and spoken English. Ability to travel to corporate headquarters as well as attend EU meetings as required This role provides hybrid working from home and a Central London office, and a strong culture with the support and opportunities to progress further into your career. Alongside this, my client also offers a comprehensive benefits package, including a generous bonus scheme, LTI s, healthcare, and a car allowance. My client are able to offer visa sponsorship and relocation support to candidates with relevant capabilities. If you have the skills required and would like to discuss the full details of the job, please contact Katie Dunbar on 952176, or apply with your CV.
Sep 24, 2022
Full time
RBW are collaborating with a leading international biotech to find an Associate Director of Regulatory Affairs Strategy, who will participate in the development and implementation of regulatory strategy for a range of therapeutic areas, including Pulmonology/Respiratory, Haematology, Diabetes and Gene therapies. The role is based in their international HQ in London. Role Responsibilities: Act as the Regional Regulatory Lead, to develop regulatory strategy for assigned products in collaboration with Global Regulatory Lead Ensure projects are appropriately prioritised and progressed in accordance with agreed regulatory plans, communicating any identified risks to project teams and Senior Management Manage the preparation and submission of technically complex regulatory submissions, with minimal supervision Provide appropriate strategic regulatory advice to Submission and Project Teams in a timely manner Keep regulatory affairs senior management informed on the status of global strategies and tactics, procedures and practices, with a focus on regulatory and policy trends in the EU Act as primary contact with Regulatory Authorities for assigned products and territories Lead local or global company process improvement initiatives Ensure all work is compliant with regulatory requirements and company policies and procedures Work with cross-department teams and key IHQ functions to achieve corporate and departmental goals and objectives. Able to plan, schedule and arrange own work activities with limited direction, exhibiting ownership and accountability for all projects and internal assignments Role Requirements: Bachelor s degree in life sciences Recent direct experience of clinical development Has led direct interactions with EMA, and national Competent Authorities on clinical development and complex regulatory submissions such as MAAs, new indications, and PIPs In-depth knowledge of regulatory landscape, including ICH and regional requirements for assigned territories and current regulatory trends Recognized as a knowledgeable resource for regulatory advice in other departments Desire to be part of a highly innovative company aimed at transforming the lives of people with serious diseases, their families and society Display solid ethics and fully comply with all regulatory, legal and industry codes of conduct Strategic ability, as evidenced by an awareness of the "big picture" strategic issues facing the business overall and positioning of local strategy relative to global and international requirements Ability to navigate and be successful in a fast-paced environment while delivering high quality results Adaptable to changing plans and able to behave independently with minimal guidance where needed, but also embraces being part of a team and working collaboratively Good interpersonal skills and ability to deal effectively with a variety of personalities Acts to promote an energizing, inclusive environment and good morale Empowers other team members through delegation of tasks and decisions Excellent communication skills, strong oral/written presentation skills. Fluent written and spoken English. Ability to travel to corporate headquarters as well as attend EU meetings as required This role provides hybrid working from home and a Central London office, and a strong culture with the support and opportunities to progress further into your career. Alongside this, my client also offers a comprehensive benefits package, including a generous bonus scheme, LTI s, healthcare, and a car allowance. My client are able to offer visa sponsorship and relocation support to candidates with relevant capabilities. If you have the skills required and would like to discuss the full details of the job, please contact Katie Dunbar on 952176, or apply with your CV.
Clinical Research Associate 2 / Senior CRA - (Regionalised) A variety of soft skills and experience may be required for the following role Please ensure you check the overview below carefully. Wales £40,000 - £55,000 (DOE) My client, a large global organisation with a vast European presence are looking for an experienced CRA to join their business as a Senior CRA or CRA II. If you are looking for an opportunity to broaden your career, work on some truly fascinating studies in very niche therapeutic areas, or even just a genuine chance of ongoing career development then I am confident this could be the perfect organisation for you. The beauty of this client is that they focus on multiple therapy areas across all phases of the clinical trial spectrum which means no matter what your previous exposure has been there could be a perfect opportunity waiting for you. New medicine development is at the forefront of everything they do, this is a truly innovative business who are constantly looking for ways to change and better the future of the life sciences industry and as a result have been listed as one of the most admired companies to work for this year. If this isn't enough to make you want to apply then its also worth mentioning that this is a company who also take their corporate social responsibilities seriously, whether that be ways to prevent pollution and carbon emissions or more simply supporting causes that are important to their employees this is at the core of what they do. As an ARC your responsibilities will include: Coordinating Phase I-IV clinical trials Performing the full range of site visits: qualification, initiation, monitoring, motivational, audit support, and close out. Identifying and conducting feasibility assessments for proposed study sites in conjunction with the Project Team. Liaising with other appropriate departments to ensure the smooth running of the study Provide guidance and leadership to more junior CRAs (Senior CRA responsibility) Your previous experience should include: A degree in life science or related and experience of independent monitoring within clinical research, including good clinical knowledge and working understanding of GCP Regulations. In addition, previous experience within any other Clinical function would be highly advantageous. This position is home based anywhere across France and therefore flexibility to travel will be essential. To know more about this terrific company and to get a better feel for whether this position falls in line with your expectations, please speak to Paul Adam using the below contact information: (0)
Sep 23, 2022
Full time
Clinical Research Associate 2 / Senior CRA - (Regionalised) A variety of soft skills and experience may be required for the following role Please ensure you check the overview below carefully. Wales £40,000 - £55,000 (DOE) My client, a large global organisation with a vast European presence are looking for an experienced CRA to join their business as a Senior CRA or CRA II. If you are looking for an opportunity to broaden your career, work on some truly fascinating studies in very niche therapeutic areas, or even just a genuine chance of ongoing career development then I am confident this could be the perfect organisation for you. The beauty of this client is that they focus on multiple therapy areas across all phases of the clinical trial spectrum which means no matter what your previous exposure has been there could be a perfect opportunity waiting for you. New medicine development is at the forefront of everything they do, this is a truly innovative business who are constantly looking for ways to change and better the future of the life sciences industry and as a result have been listed as one of the most admired companies to work for this year. If this isn't enough to make you want to apply then its also worth mentioning that this is a company who also take their corporate social responsibilities seriously, whether that be ways to prevent pollution and carbon emissions or more simply supporting causes that are important to their employees this is at the core of what they do. As an ARC your responsibilities will include: Coordinating Phase I-IV clinical trials Performing the full range of site visits: qualification, initiation, monitoring, motivational, audit support, and close out. Identifying and conducting feasibility assessments for proposed study sites in conjunction with the Project Team. Liaising with other appropriate departments to ensure the smooth running of the study Provide guidance and leadership to more junior CRAs (Senior CRA responsibility) Your previous experience should include: A degree in life science or related and experience of independent monitoring within clinical research, including good clinical knowledge and working understanding of GCP Regulations. In addition, previous experience within any other Clinical function would be highly advantageous. This position is home based anywhere across France and therefore flexibility to travel will be essential. To know more about this terrific company and to get a better feel for whether this position falls in line with your expectations, please speak to Paul Adam using the below contact information: (0)
Regional Clinical Research Associate ll The full job description covers all associated skills, previous experience, and any qualifications that applicants are expected to have. £40k - £50k (D.O.E.) Generous Car Allowance, Sign-On Bonus To be based in either London, Bristol, Swindon, Wales, Dublin, Belfast At RBW we pride ourselves in taking time to understand our candidates and offer not only a true consultative approach but also, really take time to understand what's important to you and make recommendations of suitable roles based on your experience, not on which role will pay the highest commission. I am currently recruiting for a 'World-Class' CRO who are looking for their next hire due to continued expansion to be based in UK/Ireland You will work within an established team who will offer you support and guidance, along with providing you with a structured training program, ensuring you are able to work autonomously, making sure to put the quality of the trial first. Due to the nature of the role, your duties will change based on requirement however below are some of the more routine duties you will perform in this role. Coordinating phase l - lV clinical trials Performing the full suite of site visits: qualification, initiation, monitoring, motivational, audit support and close out Identifying and conducting feasibility assessments for proposed study sites in accordance with the Project team Liaising with other departments to ensure smooth running of the study Reporting on serious adverse events Checking drug accountability Previous Experience: Life Science degree or equivalent Willingness to travel Driving License Excellent communication and interpersonal skills Extensive SIV/IMV/COV 18-24 months on-site, independent monitoring experience. If you think your experience and career aspirations match the above positions, I would be very interested in hearing from you. Please call or email Paul on / (mailto:364079/)
Sep 23, 2022
Full time
Regional Clinical Research Associate ll The full job description covers all associated skills, previous experience, and any qualifications that applicants are expected to have. £40k - £50k (D.O.E.) Generous Car Allowance, Sign-On Bonus To be based in either London, Bristol, Swindon, Wales, Dublin, Belfast At RBW we pride ourselves in taking time to understand our candidates and offer not only a true consultative approach but also, really take time to understand what's important to you and make recommendations of suitable roles based on your experience, not on which role will pay the highest commission. I am currently recruiting for a 'World-Class' CRO who are looking for their next hire due to continued expansion to be based in UK/Ireland You will work within an established team who will offer you support and guidance, along with providing you with a structured training program, ensuring you are able to work autonomously, making sure to put the quality of the trial first. Due to the nature of the role, your duties will change based on requirement however below are some of the more routine duties you will perform in this role. Coordinating phase l - lV clinical trials Performing the full suite of site visits: qualification, initiation, monitoring, motivational, audit support and close out Identifying and conducting feasibility assessments for proposed study sites in accordance with the Project team Liaising with other departments to ensure smooth running of the study Reporting on serious adverse events Checking drug accountability Previous Experience: Life Science degree or equivalent Willingness to travel Driving License Excellent communication and interpersonal skills Extensive SIV/IMV/COV 18-24 months on-site, independent monitoring experience. If you think your experience and career aspirations match the above positions, I would be very interested in hearing from you. Please call or email Paul on / (mailto:364079/)
Geoff King at RBW Consulting is working with an international, full service CRO in the recruitment of a Senior Data Manager to work as part of the global multi sponsor team. Established over 20 years ago this and now operating across the globe, this full service CRO provide premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. As Senior Data Manager you will have the opportunity to join a remote team of Data Managers based across Europe working on phase 1-4 clinical trials in multiple therapeutic areas including Oncology, Haematology, CNS, Rare Disease and more. The Senior Clinical Data Manager reports to the Data Management Coordinator, serves as primary point of contact to the study team for clinical data related matters and ensure clinical data is managed in compliance with applicable standards, regulatory guidelines and company SOPs. *Main duties & responsibilities:* * Ensure data is managed in compliance with applicable standards (e.g. CDISC), regulatory guidelines and SOPs; * Prepare Data Management documents (CRF, Data Management Plan, Data transfer specifications, etc.) * Design the paper and/or electronic Case Report Forms (CRF), including paper PROs (diaries, questionnaires), in co-operation with the Sponsor, and the study team. * Prepare and validate the eCRF/clinical databases and related tools. * Manage database locks and freezing before data analysis. * Prepare, maintain, and archive data management documentation. * Liaise with Sponsor and external stakeholders regarding data management activities. *Key requirements:* * Min. 3 years' experience within Data Management * Digital skills and good knowledge of FDA 21 CFR Part 11 and system validation; * Solid knowledge on relational databases and programming languages; * Knowledge of CDISC standard specifications; * English language (fluent reading, writing and verbal skills); A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Dec 08, 2021
Full time
Geoff King at RBW Consulting is working with an international, full service CRO in the recruitment of a Senior Data Manager to work as part of the global multi sponsor team. Established over 20 years ago this and now operating across the globe, this full service CRO provide premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. As Senior Data Manager you will have the opportunity to join a remote team of Data Managers based across Europe working on phase 1-4 clinical trials in multiple therapeutic areas including Oncology, Haematology, CNS, Rare Disease and more. The Senior Clinical Data Manager reports to the Data Management Coordinator, serves as primary point of contact to the study team for clinical data related matters and ensure clinical data is managed in compliance with applicable standards, regulatory guidelines and company SOPs. *Main duties & responsibilities:* * Ensure data is managed in compliance with applicable standards (e.g. CDISC), regulatory guidelines and SOPs; * Prepare Data Management documents (CRF, Data Management Plan, Data transfer specifications, etc.) * Design the paper and/or electronic Case Report Forms (CRF), including paper PROs (diaries, questionnaires), in co-operation with the Sponsor, and the study team. * Prepare and validate the eCRF/clinical databases and related tools. * Manage database locks and freezing before data analysis. * Prepare, maintain, and archive data management documentation. * Liaise with Sponsor and external stakeholders regarding data management activities. *Key requirements:* * Min. 3 years' experience within Data Management * Digital skills and good knowledge of FDA 21 CFR Part 11 and system validation; * Solid knowledge on relational databases and programming languages; * Knowledge of CDISC standard specifications; * English language (fluent reading, writing and verbal skills); A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Geoff King at RBW Consulting is working with an international, full service CRO in the recruitment of a Senior Statistical Programmer to work as part of the global multi sponsor team. Established over 20 years ago and now operating across the globe, this full service CRO provide trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of global clinical studies. The Senior SAS Programmer is responsible for leading studies and developing SAS programs, generating datasets, tables, figures and lists for clinical trials, publication requests and health authorities. *Main duties & responsibilities:* * Be the CDISC SDTM/ADaM expert; follow CDISC guidelines to generate SDTM datasets and related documents; * Develop standard SAS macros and prepare the corresponding validation documents; * Perform quality check on SAS programs/outputs created by another Statistician/SAS Programmer; * Develop SAS programs/macros and utilities for data cleaning: * Develop and validate SAS programs for identification of Protocol Deviations; * Prepare, maintain, and archive of SAS programming documentation; * Contribute to on-boarding of new associates and act as a mentor for junior staff; * Keep informed on new SAS developments relevant to the clinical trial data management. *Key requirements:* * Degree in relevant area * 3+ years experience in SAS Programming within Life Science industry * Knowledge and expertise in statistics and its applications to clinical trials; * Solid knowledge of SAS and CDISC; * Digital skills and good knowledge of FDA 21 CFR Part 11 and system validation; * Solid knowledge of SAS and experience in developing CDISC standard specifications and datasets (SDTM); * Fluent in English; A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Dec 08, 2021
Full time
Geoff King at RBW Consulting is working with an international, full service CRO in the recruitment of a Senior Statistical Programmer to work as part of the global multi sponsor team. Established over 20 years ago and now operating across the globe, this full service CRO provide trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of global clinical studies. The Senior SAS Programmer is responsible for leading studies and developing SAS programs, generating datasets, tables, figures and lists for clinical trials, publication requests and health authorities. *Main duties & responsibilities:* * Be the CDISC SDTM/ADaM expert; follow CDISC guidelines to generate SDTM datasets and related documents; * Develop standard SAS macros and prepare the corresponding validation documents; * Perform quality check on SAS programs/outputs created by another Statistician/SAS Programmer; * Develop SAS programs/macros and utilities for data cleaning: * Develop and validate SAS programs for identification of Protocol Deviations; * Prepare, maintain, and archive of SAS programming documentation; * Contribute to on-boarding of new associates and act as a mentor for junior staff; * Keep informed on new SAS developments relevant to the clinical trial data management. *Key requirements:* * Degree in relevant area * 3+ years experience in SAS Programming within Life Science industry * Knowledge and expertise in statistics and its applications to clinical trials; * Solid knowledge of SAS and CDISC; * Digital skills and good knowledge of FDA 21 CFR Part 11 and system validation; * Solid knowledge of SAS and experience in developing CDISC standard specifications and datasets (SDTM); * Fluent in English; A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Geoff King at RBW Consulting is working with a leading CRO in the recruitment of multiple Senior Data Managers to work with one of their key pharmaceutical clients. As Senior Data Manager you will have the opportunity to join a well-established team of over 30 Data Managers outsourced to work exclusively for a global pharmaceutical company. You will be responsible for the implementation and development of phase 1-4 clinical trials in specific therapeutic areas including Cardiology, Ophthalmology, Oncology, Neurology and more. Reporting to the Associate Director of Global Data Management you will have oversight of project deliverables, manage key study metrics, lead a team of UK and EU Clinical Data Associates, manage internal stakeholders and external vendors for the pharmaceutical client. Knowledge of Medidata Rave is preferred but not essential. *Main duties & responsibilities:* * Developing, implementing and maintaining the Data Management Plan * Execution of data validation plans * Reporting on the status of projects and tasks * Proposing solutions to process and technical issues * Ensuring timely generation and tracking of data queries * Interacting with the sites, CRA's and Lead CDC's * Reconciliation of external data *Key requirements:* * Min. 3 years' experience within Data Management * Management and team leadership skills necessary to lead a data management team. * Proven project delivery skills. * Excellent time management, people management and communication skills. * Educated to degree level (preferably Life Science) * Knowledge of Medidata Rave A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Dec 08, 2021
Full time
Geoff King at RBW Consulting is working with a leading CRO in the recruitment of multiple Senior Data Managers to work with one of their key pharmaceutical clients. As Senior Data Manager you will have the opportunity to join a well-established team of over 30 Data Managers outsourced to work exclusively for a global pharmaceutical company. You will be responsible for the implementation and development of phase 1-4 clinical trials in specific therapeutic areas including Cardiology, Ophthalmology, Oncology, Neurology and more. Reporting to the Associate Director of Global Data Management you will have oversight of project deliverables, manage key study metrics, lead a team of UK and EU Clinical Data Associates, manage internal stakeholders and external vendors for the pharmaceutical client. Knowledge of Medidata Rave is preferred but not essential. *Main duties & responsibilities:* * Developing, implementing and maintaining the Data Management Plan * Execution of data validation plans * Reporting on the status of projects and tasks * Proposing solutions to process and technical issues * Ensuring timely generation and tracking of data queries * Interacting with the sites, CRA's and Lead CDC's * Reconciliation of external data *Key requirements:* * Min. 3 years' experience within Data Management * Management and team leadership skills necessary to lead a data management team. * Proven project delivery skills. * Excellent time management, people management and communication skills. * Educated to degree level (preferably Life Science) * Knowledge of Medidata Rave A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Geoff King at RBW Consulting is working with one of the world's leading CRO in the recruitment of multiple Senior & Principal Statistical Programmers as they embark on an exciting new era of Data Science in the world of healthcare and drug discovery. Supported by cutting edge technology and a management team of industry recognised experts this organisation gives you the opportunity to work at the forefront of the pharmaceutical industry by leading assigned trials as part of a specialist, single sponsor team on multiple global studies across phases I - IV. Able to be worked from home across Europe there are fantastic promotional opportunities thanks to the industry leading training and development on offer. Career paths range from line management to subject matter expert and will be tailored specifically to you. With continued plans for expansion and Human Data Science at the forefront of this multi-billion pound company Statistical Programming is integral to everything they do. Therefore, there are opportunities across Europe at both Senior and Principal levels. *Main duties & responsibilities:* * Import data from various sources * Program quality control checks for source data and reporting data issues * Interpret project level requirements and develop programming specifications * Write programming code following established Good Programming Practices * Program SDTM and ADaM datasets * Program to create statistical analysis tables, listing and figures * Validate datasets and all statistical outputs per prescribed gate checks * Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines * Use and promote the use of established standards, SOPs, and standard methodologies * Provide training and mentoring to team members and department staff *Key requirements:* * Statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology industries * Knowledge of statistics, programming and/or clinical drug development process * Advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language * Ability to lead teams and projects and capable of managing at a group level * Degree in computer science or related field and 3 years relevant experience A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Dec 07, 2021
Full time
Geoff King at RBW Consulting is working with one of the world's leading CRO in the recruitment of multiple Senior & Principal Statistical Programmers as they embark on an exciting new era of Data Science in the world of healthcare and drug discovery. Supported by cutting edge technology and a management team of industry recognised experts this organisation gives you the opportunity to work at the forefront of the pharmaceutical industry by leading assigned trials as part of a specialist, single sponsor team on multiple global studies across phases I - IV. Able to be worked from home across Europe there are fantastic promotional opportunities thanks to the industry leading training and development on offer. Career paths range from line management to subject matter expert and will be tailored specifically to you. With continued plans for expansion and Human Data Science at the forefront of this multi-billion pound company Statistical Programming is integral to everything they do. Therefore, there are opportunities across Europe at both Senior and Principal levels. *Main duties & responsibilities:* * Import data from various sources * Program quality control checks for source data and reporting data issues * Interpret project level requirements and develop programming specifications * Write programming code following established Good Programming Practices * Program SDTM and ADaM datasets * Program to create statistical analysis tables, listing and figures * Validate datasets and all statistical outputs per prescribed gate checks * Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines * Use and promote the use of established standards, SOPs, and standard methodologies * Provide training and mentoring to team members and department staff *Key requirements:* * Statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology industries * Knowledge of statistics, programming and/or clinical drug development process * Advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language * Ability to lead teams and projects and capable of managing at a group level * Degree in computer science or related field and 3 years relevant experience A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Are you a creative, strategic, and enthusiastic PR Director looking for an opportunity to shape and lead a pharmaceutical communications team? Reporting to the Managing Director, you will be a vital part of the Senior Leadership Team driving the continued success of this award-winning, independent healthcare communications agency. *Key Responsibilities:* * As a member of the Senior Leadership Team, you will be key to shaping the company's strategy and business plan. * Develop strong and meaningful relationships with clients, acting as the strategic lead, proactively providing insight and advice. * Generating new business and growth of current client accounts. * Lead and manage the team, ensuring continued development and growth of junior staff members. *You are:* * Experienced working in a healthcare communications agency. * Entrepreneurial, naturally seeking out new business opportunities with the proven success of winning new business. * Experienced in PR Communications. * A great leader, offering guidance and support. * Strategic in your planning and execution of tasks. * An expert in the field of Pharmaceutical Communications. My client is an independent award-winning health communications consultancy with a true focus on patients. Specialising in healthcare communications, public affairs, and patient advocacy. With a small but experienced team, they offer a friendly, dynamic, and welcoming environment where everyone has the wellbeing of patients at the heart of everything they do. Alongside a generous salary and benefits package, the agency offers a substantial new business incentive scheme, flexible working, and great company social events. For more information please contact Nicky Stunt, Healthcare Communications Consultant at RBW Consulting.
Dec 06, 2021
Full time
Are you a creative, strategic, and enthusiastic PR Director looking for an opportunity to shape and lead a pharmaceutical communications team? Reporting to the Managing Director, you will be a vital part of the Senior Leadership Team driving the continued success of this award-winning, independent healthcare communications agency. *Key Responsibilities:* * As a member of the Senior Leadership Team, you will be key to shaping the company's strategy and business plan. * Develop strong and meaningful relationships with clients, acting as the strategic lead, proactively providing insight and advice. * Generating new business and growth of current client accounts. * Lead and manage the team, ensuring continued development and growth of junior staff members. *You are:* * Experienced working in a healthcare communications agency. * Entrepreneurial, naturally seeking out new business opportunities with the proven success of winning new business. * Experienced in PR Communications. * A great leader, offering guidance and support. * Strategic in your planning and execution of tasks. * An expert in the field of Pharmaceutical Communications. My client is an independent award-winning health communications consultancy with a true focus on patients. Specialising in healthcare communications, public affairs, and patient advocacy. With a small but experienced team, they offer a friendly, dynamic, and welcoming environment where everyone has the wellbeing of patients at the heart of everything they do. Alongside a generous salary and benefits package, the agency offers a substantial new business incentive scheme, flexible working, and great company social events. For more information please contact Nicky Stunt, Healthcare Communications Consultant at RBW Consulting.
Marketing Executive - Digital Location: London / remote working Salary: £30-40,0000 pa plus benefits Our client is a leading provider of software and data analytics to the life science sector. Due to UK team growth we are looking for an experienced Digital Marketing Executive to join their team. Ultimately this role will involve using your digital marketing expertise to evolve our clients digital channels and generate new commercial opportunities. *Key responsibilities will typically include -* * Creating and evolving on-site commercial opportunities (advertising, sponsorship, hosted content, etc.) * Acting as a key team member to help drive the acquisition of our clients members and increase engagement of existing members through developing and implementing user experience (UX) and conversion rate optimisation (CRO) plans, including activities such as A/B testing, funnel analysis, and attribution modelling * Contribute to optimising client campaign performance and ROI data, by using and integrating our analytics platforms * Develop and maintain business development collateral (media pack, key stats) * Work closely with the Head of Digital to establish a reporting framework to supply actionable insights regarding Editorial and Acquisition teams and enable them to deliver effective data-driven content production and marketing tactics * Supporting the digital team creating and executing social media plans to help raise brand awareness and drive member acquisition and engagement * Support with the delivery of client omnichannel programmes across key company channels, including email and data collection platforms. * Explore new commercial opportunities We are particularly interested in speaking to experienced digital marketing professionals from a digital role client side in pharma or who have worked for a progressive marketing/creative healthcare agency, however also keen to speak to digital marketing professionals who have worked in a SaaS, financial or oil and gas environment. This is an exciting time to join this growing sector. For further information please contact Louise directly on (0)
Dec 05, 2021
Full time
Marketing Executive - Digital Location: London / remote working Salary: £30-40,0000 pa plus benefits Our client is a leading provider of software and data analytics to the life science sector. Due to UK team growth we are looking for an experienced Digital Marketing Executive to join their team. Ultimately this role will involve using your digital marketing expertise to evolve our clients digital channels and generate new commercial opportunities. *Key responsibilities will typically include -* * Creating and evolving on-site commercial opportunities (advertising, sponsorship, hosted content, etc.) * Acting as a key team member to help drive the acquisition of our clients members and increase engagement of existing members through developing and implementing user experience (UX) and conversion rate optimisation (CRO) plans, including activities such as A/B testing, funnel analysis, and attribution modelling * Contribute to optimising client campaign performance and ROI data, by using and integrating our analytics platforms * Develop and maintain business development collateral (media pack, key stats) * Work closely with the Head of Digital to establish a reporting framework to supply actionable insights regarding Editorial and Acquisition teams and enable them to deliver effective data-driven content production and marketing tactics * Supporting the digital team creating and executing social media plans to help raise brand awareness and drive member acquisition and engagement * Support with the delivery of client omnichannel programmes across key company channels, including email and data collection platforms. * Explore new commercial opportunities We are particularly interested in speaking to experienced digital marketing professionals from a digital role client side in pharma or who have worked for a progressive marketing/creative healthcare agency, however also keen to speak to digital marketing professionals who have worked in a SaaS, financial or oil and gas environment. This is an exciting time to join this growing sector. For further information please contact Louise directly on (0)
*Senior Clinical Operations Manager* *UK - £60 - £70k* Working with a Small/Mid-sized CRO, due to expansion, my client are looking for a Senior Clinical Operations Manager. You will report to the Head of Clinical Operations and will support the operation by reviewing and forecasting staffing requirements, analyse metrics encouraging KPI's to be met and implement improvements based on KPI data. You will be involved in ensuring the completion of company training and to provide senior support and oversight to direct reports which will include CSM's and CPM's, SCRM and CRA's. Working closely with senior members of the team, you will also be responsible for evaluating study proposals and RFPs to maintain an adequate resource cover for projects. You will also be responsible for undertaking the recruitment and selection activities and work closely with the HR Manager to ensure that staff metrics and staff reporting is undertaken. This will also involve preparing feedback and evaluation reports concerning probation of new staff, appraisals, 1-1's and 360 reviews. A strong and supportive team culture is very high on the agenda and you will be tasked to think of new processes and create a team environment which supports and follows company standards. *Other Tasks Include but are not limited to:* * Working alongside Head of QA to identify and implement new Clin Ops Processes * Work with the Financial Controller supporting operational budgeting * Interacting and communicating with executive leaderships such as CEOs, COOs, Directors, Professors and Consultants * Undertake line management duties for direct reports as required * Completion of time-sheet *The Person: * * 5years + experience within a senior clinical operations role/ (pharma/biotech/NHS) (or equivalent) * Min of 4 years + demonstrated experience of line management * Well versed knowledge of clinical operations, clinical site activity, the monitoring process and study management * Experience of managing study and department budgets * An absolute eye for detail * Willingness to travel when required * Experienced in multiple therapeutic areas with extensive exposure to complex studies and protocols being an advantage * Will strive to improve functional and study team ways of working and share best practice across coordinators * Life Science Degree of equivalent If you are interested in applying to this role and would like to discuss your application, please contact Paul on or send your CV to [](mailto:)
Dec 05, 2021
Full time
*Senior Clinical Operations Manager* *UK - £60 - £70k* Working with a Small/Mid-sized CRO, due to expansion, my client are looking for a Senior Clinical Operations Manager. You will report to the Head of Clinical Operations and will support the operation by reviewing and forecasting staffing requirements, analyse metrics encouraging KPI's to be met and implement improvements based on KPI data. You will be involved in ensuring the completion of company training and to provide senior support and oversight to direct reports which will include CSM's and CPM's, SCRM and CRA's. Working closely with senior members of the team, you will also be responsible for evaluating study proposals and RFPs to maintain an adequate resource cover for projects. You will also be responsible for undertaking the recruitment and selection activities and work closely with the HR Manager to ensure that staff metrics and staff reporting is undertaken. This will also involve preparing feedback and evaluation reports concerning probation of new staff, appraisals, 1-1's and 360 reviews. A strong and supportive team culture is very high on the agenda and you will be tasked to think of new processes and create a team environment which supports and follows company standards. *Other Tasks Include but are not limited to:* * Working alongside Head of QA to identify and implement new Clin Ops Processes * Work with the Financial Controller supporting operational budgeting * Interacting and communicating with executive leaderships such as CEOs, COOs, Directors, Professors and Consultants * Undertake line management duties for direct reports as required * Completion of time-sheet *The Person: * * 5years + experience within a senior clinical operations role/ (pharma/biotech/NHS) (or equivalent) * Min of 4 years + demonstrated experience of line management * Well versed knowledge of clinical operations, clinical site activity, the monitoring process and study management * Experience of managing study and department budgets * An absolute eye for detail * Willingness to travel when required * Experienced in multiple therapeutic areas with extensive exposure to complex studies and protocols being an advantage * Will strive to improve functional and study team ways of working and share best practice across coordinators * Life Science Degree of equivalent If you are interested in applying to this role and would like to discuss your application, please contact Paul on or send your CV to [](mailto:)
*HR / Human Resources Director - Healthtech* *Location: UK, London* *£100-120k plus excellent bonus and benefits package. * Our client a rapidly growing Healthtech company is looking for an experienced Human Resources Director to join its growing UK team. This is an exciting opportunity for an HR Director who enjoys building HR strategies from scratch and working in a fast-changing environment. Our client is months away from FDA approval with an imminent IPO. *Who are we looking for?* You are a senior level HR professional with solid generalist UK HR experience having previously worked for a technology company and possibly already successfully helped with company expansion into Europe. You will have an excellent reputation as an HR leader with solid experience building and managing recruitment processes. You will also have been involved in effectively creating competitive benefits and compensation packages to help attract the best to the company while effectively liaising with UK leadership teams on all HR related issues being the go to person regarding all matters related to UK employment law. *Typical responsibilities will involve* * Act as Business Partner and Advisor to the UK leadership team on all HR Issues (OD, strategy, hiring, compensation and benefits) * Lead Learning and Development and performance processes * Manage UK employee relations * Produce and Lead a recruitment plan to attract the best talent * Build and lead a team of HR professionals * Shape employee experience including onboarding and offboarding, events and celebrations. This is a senior level position reporting directly to the Country Manager. CIPD level 5 or 7 a definite advantage as well as having previously worked within the technology sector for a start-up. Great role for an experienced, intelligent people driven HR Leader. Our clients UK office is based in central London with the requirement to be in the office potentially 2/3 days a week. Very competitive salary package. For further information please contact Louise on (0)
Dec 04, 2021
Full time
*HR / Human Resources Director - Healthtech* *Location: UK, London* *£100-120k plus excellent bonus and benefits package. * Our client a rapidly growing Healthtech company is looking for an experienced Human Resources Director to join its growing UK team. This is an exciting opportunity for an HR Director who enjoys building HR strategies from scratch and working in a fast-changing environment. Our client is months away from FDA approval with an imminent IPO. *Who are we looking for?* You are a senior level HR professional with solid generalist UK HR experience having previously worked for a technology company and possibly already successfully helped with company expansion into Europe. You will have an excellent reputation as an HR leader with solid experience building and managing recruitment processes. You will also have been involved in effectively creating competitive benefits and compensation packages to help attract the best to the company while effectively liaising with UK leadership teams on all HR related issues being the go to person regarding all matters related to UK employment law. *Typical responsibilities will involve* * Act as Business Partner and Advisor to the UK leadership team on all HR Issues (OD, strategy, hiring, compensation and benefits) * Lead Learning and Development and performance processes * Manage UK employee relations * Produce and Lead a recruitment plan to attract the best talent * Build and lead a team of HR professionals * Shape employee experience including onboarding and offboarding, events and celebrations. This is a senior level position reporting directly to the Country Manager. CIPD level 5 or 7 a definite advantage as well as having previously worked within the technology sector for a start-up. Great role for an experienced, intelligent people driven HR Leader. Our clients UK office is based in central London with the requirement to be in the office potentially 2/3 days a week. Very competitive salary package. For further information please contact Louise on (0)
I am currently partnered with a globally recognised CRO looking for an experienced CRA to join their team on an initial 6 month contract as Senior CRA, this company focus on R&D across niche indications within Oncology. * Senior CRA for global CRO * Initial 6 month contract * Oncology experience essential * 1.0FTE for Dec/Jan start If this could be of interest to you or anyone in your network then please get in touch to discuss more details, you can reach me directly on
Dec 04, 2021
Full time
I am currently partnered with a globally recognised CRO looking for an experienced CRA to join their team on an initial 6 month contract as Senior CRA, this company focus on R&D across niche indications within Oncology. * Senior CRA for global CRO * Initial 6 month contract * Oncology experience essential * 1.0FTE for Dec/Jan start If this could be of interest to you or anyone in your network then please get in touch to discuss more details, you can reach me directly on
Geoff King at RBW Consulting is recruiting for a Lead Statistical Programmer to join one of the world's leading independent biotechnology companies to oversee third party vendors and clinical research organisations bring the exciting product pipeline to market. As Lead Statistical Programmer (Principal level) you will join an existing global team of programmers across the UK, Europe and US who are responsible for overseeing, mentoring and leading the team of CRO statistical programmers who work across multiple therapeutic area's including Oncology, Cardiovascular and Inflammatory Disease. Along with strong technical ability with CDSIC SDTM & ADaM, datasets, review outputs and datasets you will be expected to be outgoing with leadership qualities to assist in project management and vendor oversight. In this vital role you will be responsible for oversight of the Functional Services Provider (FSP) focusing on operational and delivery projects to the expected levels of high quality and compliance. *Main duties & responsibilities:* * Ensure team programming meets quality, compliance, timeliness, and productivity expectations * Ensure team adheres to relevant SOPs and other controlled documents * Provide guidance to Study Lead Programmers on Global Statistical Programming (GSP) processes, tools, and utilities * Contribute to team onboarding training material development and revisions, and support the initial training of team staff * Contribute to team performance metrics development, data collection and reporting *Key requirements:* * BSc in Mathematics, Statistics, Computer Science or related field * SAS programming experience working within a clinical trials environment (Pharma, CRO or biotech) * Knowledge of CDSIC standards and industry best practices * Familiarity with R or Python * Excellent written and verbal communication skills * Ability to communicate with a broad range of people across different functions A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Dec 04, 2021
Full time
Geoff King at RBW Consulting is recruiting for a Lead Statistical Programmer to join one of the world's leading independent biotechnology companies to oversee third party vendors and clinical research organisations bring the exciting product pipeline to market. As Lead Statistical Programmer (Principal level) you will join an existing global team of programmers across the UK, Europe and US who are responsible for overseeing, mentoring and leading the team of CRO statistical programmers who work across multiple therapeutic area's including Oncology, Cardiovascular and Inflammatory Disease. Along with strong technical ability with CDSIC SDTM & ADaM, datasets, review outputs and datasets you will be expected to be outgoing with leadership qualities to assist in project management and vendor oversight. In this vital role you will be responsible for oversight of the Functional Services Provider (FSP) focusing on operational and delivery projects to the expected levels of high quality and compliance. *Main duties & responsibilities:* * Ensure team programming meets quality, compliance, timeliness, and productivity expectations * Ensure team adheres to relevant SOPs and other controlled documents * Provide guidance to Study Lead Programmers on Global Statistical Programming (GSP) processes, tools, and utilities * Contribute to team onboarding training material development and revisions, and support the initial training of team staff * Contribute to team performance metrics development, data collection and reporting *Key requirements:* * BSc in Mathematics, Statistics, Computer Science or related field * SAS programming experience working within a clinical trials environment (Pharma, CRO or biotech) * Knowledge of CDSIC standards and industry best practices * Familiarity with R or Python * Excellent written and verbal communication skills * Ability to communicate with a broad range of people across different functions A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Our client is a business with a purpose: Reducing the mortality rate of patients with cancer through early detection. They are developing a non-invasive, blood-based diagnostic for the early detection of cancer. Their test analyses cancer-driven metabolic activity in blood, which their AI software is trained to then interpret and diagnose- amazing right?! They are beginning the regulatory journey to market supported by a highly specialised regulatory consultancy team. This unique offering brings together innovative IVD hardware with AI software platforms as medical devices, at a challenging time of regulatory change for the UK and the EU. We are therefore seeking a Senior Quality Specialist or Quality Manager with prior experience of laboratory based QMS and IVD, who wants to help build a successful business. This person will work with technical and data scientists, clinicians, technicians and directors to map out the process from sampling to reporting. Reporting to the CEO, this person will select and build the Quality Management System to underpin the journey to UKCA/CE marking for the technology. *Key Objectives:* * To set up and maintain a suitable Quality Management System to ISO 13485:2016 * To assist with development and updates to the Quality Manual * To direct processes and procedures to set up the laboratory to ISO 15189 * To assist with external auditor procedures and conduct internal audits of the Quality Management System including Quality Procedures and the SOP system. *Key Responsibilities:* * Setting up of an appropriate EN ISO 13485 and EN 62304 compliant quality management system to support regulatory objectives * Close working relationship with developers, scientists and technician staff to instruct in the requirements and standard expected within a QMS * Keep up to date with QMS legislative changes * Responsible for the continued implementation and maintenance of the QMS described in the quality manual * Identify and record problems concerning products, processes and systems, and implementing and verifying solutions * Manage company activities to control the processing and prevent delivery of non-conforming products * Ensure that processes needed for the QMS are established, implemented and maintained * Report to directors on the performance of the QMS and suggesting improvements * Promote awareness of regulatory requirements throughout the organisation *Desirable Knowledge, Skills and Experience : * * Strong evidence of setting up and managing a QMS * Experience of working in the IVD medical device field, implementing the requirements of ISO 13485:2016 *AND/OR* experience of working with software life cycle QMS (ISO 13485) or IEC62304:2006 * Good working knowledge of the MDD 93/42/EEC and IVDD 98/79/EEC regulations and current transitional arrangements * Experience of working with notified/regulatory bodies eg MHRA and BSI * Evidence of working to highest standard independently, with superior organisational abilities * Excellent communication skills including the ability to explain quality management effectively and engage with various disciplines- scientists, technicians and business * Motivated and inspired with an innovative approach to work This is a fabulous opportunity to be part of a growing award-winning organisation focussed on patient outcomes. Salary and benefits are negotiable based on experience, and the role will be based from home with occasional trips to the office in Swansea. If you are excited by working in a company with a vision that you can help shape, and feel your values are aligned, please apply today or contact Katie Dunbar on 952176 for more information.
Dec 04, 2021
Full time
Our client is a business with a purpose: Reducing the mortality rate of patients with cancer through early detection. They are developing a non-invasive, blood-based diagnostic for the early detection of cancer. Their test analyses cancer-driven metabolic activity in blood, which their AI software is trained to then interpret and diagnose- amazing right?! They are beginning the regulatory journey to market supported by a highly specialised regulatory consultancy team. This unique offering brings together innovative IVD hardware with AI software platforms as medical devices, at a challenging time of regulatory change for the UK and the EU. We are therefore seeking a Senior Quality Specialist or Quality Manager with prior experience of laboratory based QMS and IVD, who wants to help build a successful business. This person will work with technical and data scientists, clinicians, technicians and directors to map out the process from sampling to reporting. Reporting to the CEO, this person will select and build the Quality Management System to underpin the journey to UKCA/CE marking for the technology. *Key Objectives:* * To set up and maintain a suitable Quality Management System to ISO 13485:2016 * To assist with development and updates to the Quality Manual * To direct processes and procedures to set up the laboratory to ISO 15189 * To assist with external auditor procedures and conduct internal audits of the Quality Management System including Quality Procedures and the SOP system. *Key Responsibilities:* * Setting up of an appropriate EN ISO 13485 and EN 62304 compliant quality management system to support regulatory objectives * Close working relationship with developers, scientists and technician staff to instruct in the requirements and standard expected within a QMS * Keep up to date with QMS legislative changes * Responsible for the continued implementation and maintenance of the QMS described in the quality manual * Identify and record problems concerning products, processes and systems, and implementing and verifying solutions * Manage company activities to control the processing and prevent delivery of non-conforming products * Ensure that processes needed for the QMS are established, implemented and maintained * Report to directors on the performance of the QMS and suggesting improvements * Promote awareness of regulatory requirements throughout the organisation *Desirable Knowledge, Skills and Experience : * * Strong evidence of setting up and managing a QMS * Experience of working in the IVD medical device field, implementing the requirements of ISO 13485:2016 *AND/OR* experience of working with software life cycle QMS (ISO 13485) or IEC62304:2006 * Good working knowledge of the MDD 93/42/EEC and IVDD 98/79/EEC regulations and current transitional arrangements * Experience of working with notified/regulatory bodies eg MHRA and BSI * Evidence of working to highest standard independently, with superior organisational abilities * Excellent communication skills including the ability to explain quality management effectively and engage with various disciplines- scientists, technicians and business * Motivated and inspired with an innovative approach to work This is a fabulous opportunity to be part of a growing award-winning organisation focussed on patient outcomes. Salary and benefits are negotiable based on experience, and the role will be based from home with occasional trips to the office in Swansea. If you are excited by working in a company with a vision that you can help shape, and feel your values are aligned, please apply today or contact Katie Dunbar on 952176 for more information.
Head of Preclinical Development - UK In partnership with our early-stage drug development client, I am recruiting for a Head of Pre-Clinical Development to advance vaccines for a range of Infectious Diseases. Our client has secured strong rounds of funding to secure the further development of their unique vaccine science towards the clinical development. To achieve this, we are searching for a head of preclinical to join this small and innovative group. This key position will see you plan and manage preclinical development programmes for vaccines, implement studies according to regulatory requirements and play a key role in development meetings for regulatory and Innovation strategies as well as helping to providing technical direction and leadership. This great opportunity will be well suited if you have experience of working in a small company environment / Start-up where you have previously provided leadership of pre-clinical developments and overseen the projects as they are outsourced to CRO / Vendor partners. This role will bring the opportunity the advance your position within the company to an even broader role in the future. A working knowledge of regulatory requirements and Quality standards will be essential is helping this group in its drug development aims. You will work alongside a small team of experts in CMC, Medical and Project Management to implement the pre-clinical development plans and devise various projects for immunological testing and assay development of vaccines. Working in a semi virtual basis, you will also manage the lab operations, manage CRO activities, set up on-going Quality systems and be part of the senior leadership team when speaking with potential company inventors. With approx. 8 - 12 years of experience in the development or Immunological / Immunotherapy and / or vaccine development from the Pharma / Biotech sector is desired. A knowledge of either Cellular Biology, Infectious diseases, Immunology will be advantageous but not essential and will allow you to fully embrace our clients' scientific platform. UK based (West) with some homebased flexibility. If you are looking to grow your career with an exciting company and be part of an amazing journey in leading Immunotherapy development and have a background in Immunology, Cellular Biology, Infectious Diseases, then drop me a line to set up a call. Simon Penrose [](mailto:)
Dec 02, 2021
Full time
Head of Preclinical Development - UK In partnership with our early-stage drug development client, I am recruiting for a Head of Pre-Clinical Development to advance vaccines for a range of Infectious Diseases. Our client has secured strong rounds of funding to secure the further development of their unique vaccine science towards the clinical development. To achieve this, we are searching for a head of preclinical to join this small and innovative group. This key position will see you plan and manage preclinical development programmes for vaccines, implement studies according to regulatory requirements and play a key role in development meetings for regulatory and Innovation strategies as well as helping to providing technical direction and leadership. This great opportunity will be well suited if you have experience of working in a small company environment / Start-up where you have previously provided leadership of pre-clinical developments and overseen the projects as they are outsourced to CRO / Vendor partners. This role will bring the opportunity the advance your position within the company to an even broader role in the future. A working knowledge of regulatory requirements and Quality standards will be essential is helping this group in its drug development aims. You will work alongside a small team of experts in CMC, Medical and Project Management to implement the pre-clinical development plans and devise various projects for immunological testing and assay development of vaccines. Working in a semi virtual basis, you will also manage the lab operations, manage CRO activities, set up on-going Quality systems and be part of the senior leadership team when speaking with potential company inventors. With approx. 8 - 12 years of experience in the development or Immunological / Immunotherapy and / or vaccine development from the Pharma / Biotech sector is desired. A knowledge of either Cellular Biology, Infectious diseases, Immunology will be advantageous but not essential and will allow you to fully embrace our clients' scientific platform. UK based (West) with some homebased flexibility. If you are looking to grow your career with an exciting company and be part of an amazing journey in leading Immunotherapy development and have a background in Immunology, Cellular Biology, Infectious Diseases, then drop me a line to set up a call. Simon Penrose [](mailto:)
RBW consulting is currently recruiting for a Principal Statistical Programmer on a permanent basis working remotely in either the UK, Belgium or Germany. The successful candidate will join a global biopharmaceutical company who strive to make the lives of people living with severe diseases that much more manageable. They continue to grow and keep their focus on the people they helping as their core value. They endeavour to deliver modern medicines and solutions that improve lives, whilst still being mindful of value. Due to continuing growth, I am seeking additional innovative minds to join my clients Statistical Programming department to help shape the future. You will be given access to cutting-edge in-house technology, allowing you to work on global projects across a variety of therapeutic areas. You will be able to progress your career in the direction you choose to go and will encourage and mentor you along the way. *Responsibilities:* * Leads and supports statistical programming activities for assigned clinical studies, submissions and development initiatives. Coordinates and provides input for assigned project and study teams on timelines and work product required to deliver high quality statistical programming services in close collaboration with CROs. * Provides a high level of effective collaboration for statistical programming initiatives with key team members within SSI and groups outside of SSI (Clinical Data Operations, Technology and Standards (CDOTS), Global Medical Writing, New Medicines, Global Clinical Project Management, therapy areas, Quantitative Clinical Pharmacology, Marketing & Market Access and Global Clinical Development & Medical Affairs) to facilitate understanding of statistical programming services and work product. * May program, validate, maintain, and document statistical analysis programs for asset development on the basis of the SAP and of other documents (Protocol, CRF, DMM, ISAP, DAP and ASD) following standard operating procedures and working documents. * Where applicable, develops innovative programming methodologies (i.e. interactive visualization, dashboards, etc.) to facilitate easier interpretation by customer base * Ensures that submission and study datasets (SDTM and ADaM), tables, figures, listings, statistical output, and program documentation meet standards requirements of regulatory agencies and other departments. * Ensures that datasets, tables, figures, listings, and statistical outputs are produced in an efficient manner, following SSI procedures and standards. Develops specification documentation for datasets (SDTM and ADaM), pooled datasets, tables, figures, listings, and associated metadata. * Supports direction, motivation, and oversight of statistical programming resources (internal and external) for timely delivery of all statistical programming outputs. Mentors and trains other statistical programmers as needed. * Ensures compliance with the 21-CFR Part 11 regulations in terms of validation of SAS programs used for statistical reporting of clinical studies. *Ideal Candidate * * Proven track record in statistical programming within the Biotechnology and/or Pharmaceutical Industry (including clinical research organizations) with proven successful track record in pharmaceutical development. * Excellent understanding and profound knowledge of statistical programming aspects required for regulatory submissions. * Expert SAS Software Programming skills, including experience with advanced DATA step, SQL and macro development to solve complex programming tasks and/or expert in other programming languages like R, or Python. Experience in Data Visualization would also be advantageous. * Advanced clinical studies design and analysis experience. * Advanced knowledge of statistical principles. Good leadership abilities and interpersonal skills to mentor and lead statistical programmers to successfully deliver high quality project, study team statistical programming work product and oversee CRO statistical programming teams To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Ashley Clarke on (0) and send your CV through using the apply button on this page.
Dec 01, 2021
Full time
RBW consulting is currently recruiting for a Principal Statistical Programmer on a permanent basis working remotely in either the UK, Belgium or Germany. The successful candidate will join a global biopharmaceutical company who strive to make the lives of people living with severe diseases that much more manageable. They continue to grow and keep their focus on the people they helping as their core value. They endeavour to deliver modern medicines and solutions that improve lives, whilst still being mindful of value. Due to continuing growth, I am seeking additional innovative minds to join my clients Statistical Programming department to help shape the future. You will be given access to cutting-edge in-house technology, allowing you to work on global projects across a variety of therapeutic areas. You will be able to progress your career in the direction you choose to go and will encourage and mentor you along the way. *Responsibilities:* * Leads and supports statistical programming activities for assigned clinical studies, submissions and development initiatives. Coordinates and provides input for assigned project and study teams on timelines and work product required to deliver high quality statistical programming services in close collaboration with CROs. * Provides a high level of effective collaboration for statistical programming initiatives with key team members within SSI and groups outside of SSI (Clinical Data Operations, Technology and Standards (CDOTS), Global Medical Writing, New Medicines, Global Clinical Project Management, therapy areas, Quantitative Clinical Pharmacology, Marketing & Market Access and Global Clinical Development & Medical Affairs) to facilitate understanding of statistical programming services and work product. * May program, validate, maintain, and document statistical analysis programs for asset development on the basis of the SAP and of other documents (Protocol, CRF, DMM, ISAP, DAP and ASD) following standard operating procedures and working documents. * Where applicable, develops innovative programming methodologies (i.e. interactive visualization, dashboards, etc.) to facilitate easier interpretation by customer base * Ensures that submission and study datasets (SDTM and ADaM), tables, figures, listings, statistical output, and program documentation meet standards requirements of regulatory agencies and other departments. * Ensures that datasets, tables, figures, listings, and statistical outputs are produced in an efficient manner, following SSI procedures and standards. Develops specification documentation for datasets (SDTM and ADaM), pooled datasets, tables, figures, listings, and associated metadata. * Supports direction, motivation, and oversight of statistical programming resources (internal and external) for timely delivery of all statistical programming outputs. Mentors and trains other statistical programmers as needed. * Ensures compliance with the 21-CFR Part 11 regulations in terms of validation of SAS programs used for statistical reporting of clinical studies. *Ideal Candidate * * Proven track record in statistical programming within the Biotechnology and/or Pharmaceutical Industry (including clinical research organizations) with proven successful track record in pharmaceutical development. * Excellent understanding and profound knowledge of statistical programming aspects required for regulatory submissions. * Expert SAS Software Programming skills, including experience with advanced DATA step, SQL and macro development to solve complex programming tasks and/or expert in other programming languages like R, or Python. Experience in Data Visualization would also be advantageous. * Advanced clinical studies design and analysis experience. * Advanced knowledge of statistical principles. Good leadership abilities and interpersonal skills to mentor and lead statistical programmers to successfully deliver high quality project, study team statistical programming work product and oversee CRO statistical programming teams To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Ashley Clarke on (0) and send your CV through using the apply button on this page.
