Real Staffing

Data Architect Opportunity (Contract) - North West of England We are excited to share an excellent opportunity for a skilled Data Architect to join our client in the Higher Education sector on a contract basis. Our client is seeking someone with expertise in data architecture and governance to contribute to impactful projects that influence their dynamic organisation click apply for full job details

Exciting Opportunity: TechnologyOne Consultant Join Our Client's Dynamic Team We are currently seeking an experienced TechnologyOne Consultant to support our client, a local government organisation based in Scotland. This contract role offers a fantastic chance to take on a pivotal position in a challenging TechnologyOne implementation project click apply for full job details

Data Architect Opportunity (Contract) - North West of England We are excited to share an excellent opportunity for a skilled Data Architect to join our client in the Higher Education sector on a contract basis. Our client is seeking someone with expertise in data architecture and governance to contribute to impactful projects that influence their dynamic organisation click apply for full job details

Solution Architect - Salesforce Join Our Client's Team in the Higher Education Sector We are currently seeking a talented and experienced Solution Architect with Salesforce expertise to join our client's dynamic team in the North West of England. This exciting contract opportunity offers the chance to make a significant impact within the higher education sector by driving end-to-end IT architecture click apply for full job details

Contract Opportunity: Exchange / M365 Cloud Engineer (2 Months) Location: Hybrid (South Coast) Duration: Initial 2 months (Immediate start preferred) Contractor / Outside IR35 We're urgently seeking an experienced Exchange Engineer or M365 Cloud Engineer to support our Modern Work Programme as we complete a critical phase of our data migration project. What You'll Be Doing: Remediating outstanding Exchange-related issues as part of our M365 migration. Working closely with internal teams to troubleshoot and resolve complex mail flow, mailbox, and legacy system challenges. Supporting a Higher Education (HE) environment - experience in this sector is highly desirable. What We're Looking For: Proven expertise in Microsoft Exchange (on-prem & online) and Microsoft 365. Strong troubleshooting and remediation skills in complex environments. Ideally, experience working in or with Higher Education institutions. Ability to hit the ground running and work independently with minimal onboarding. Why Join Us? Be part of a high-impact programme modernising our digital workplace. Collaborate with a skilled and supportive team. Flexible working with a fast-paced, delivery-focused environment. Please note that you will receive a Key Information Document if selected; the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy Registered office 8 Bishopsgate, London, EC2N 4BQ, United Kingdom Partnership Number OC387148 England and Wales

One of our top medical device clients is looking for a Validation Engineer for a 9 month contract. They are looking for a good all-rounder and seasoned engineer with a GMP background who can act as a mentor and validation lead for their existing staff members. The position is based at a diagnostics company out of Sterling manufacturing lateral flow tests...... click apply for full job details

Our client is a leader in real world data (RWD/RWE) and research solutions for healthcare and life sciences. The company is part of a global group and they work with clinical data from the UK, USA and increasingly focus on EU. The Data Scientist is a key member of the Delivery Team (Analysts, Modelers, Developers), supporting and ensuring the successful completion of research projects, healthcare-related software and other products and services for the improvement of healthcare and access to medicines. Responsibilities Develop novel use cases, design and run projects, research new algorithms, and find new ways of helping to improve clinical outcomes, productivity and research using healthcare data (e.g. HES, CPRD etc.) including study methodology, statistical methods, visualisations and machine learning techniques. Help design, develop and transform ideas (including specifications, codes and other research requirements) into deliverable projects using deep learning, machine learning and analytical techniques. The Data Scientist will interact with sales and clients to understand business challenges, develop use cases and solutions and help customers implement DL/ML algorithms and cloud technologies to solve problems. Translate client need to a scoping/protocol document for the Delivery Team with clear deliverables. Communicate key insights and findings to the delivery team and to clients through designing output documents such as visualizations, reports and models. Support the delivery team for clarification and refinement of project specifications to ensure adherence to the project scope, research principles, and regulatory obligations The Data Scientist will Program study methodology into interfaces including R, SQL, Python Evaluate risks and prediction of potential problems in research projects Support the development of research methodologies, data sources, algorithms, research output for the current and targeted clients. Qualifications/Knowledge: Training in either Epidemiology/Medical Statistics/Data Science or a relevant qualification involving numerical analysis and/or health research. Healthcare Data Analysis (desirable) Developing and testing algorithms, models and research study reports. Ideally epidemiological or other scientific studies Statistical methodology and study design (e.g. inferential statistics, regression and modelling, demographics, prevalence and incidence). Data management, cloud data storage, analysis and presentation, using healthcare databases and statistical analysis software packages (e.g. Microsoft excel, SQL and R) To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

JOB TITLE: Senior Principal Consultant, Market Access Industry: Pharmaceutical / Life-science consultancy IMPACT OF THE ROLE We provide clients from the pharmaceutical, medical device and diagnostics sectors with a broad range of payer research, pricing, reimbursement and market access strategy support. Within the Market Access space, we are a leading player, with experts across Europe, the US and APAC. As a senior member of the leadership team, you'll be working closely with the client and project team colleagues to deliver Market Access solutions, and you will be instrumental in executing the Market Access plan. This will be achieved through effective project and client management, team leadership, business development, strategic planning and analysis, recommendation and conclusion forming. WHAT WILL I BE DOING: Lead teams of Consultants in the successful delivery of projects in areas of: Payer and multi-stakeholder insight Value proposition development Market access strategy Pricing and reimbursement Drive client engagement and business development activities: Conduct competitor intelligence, benchmarking and service provision analyses Make new client contacts, follow-up leads and participate in new business meetings Ambassador for strong 'client experience' Experienced at building strong client relationships Leads proposal development, crafting a solution that meets client needs Participate in collaborative bid teams Take a role in presenting at conferences Execute projects to a client ready standard: Actively sharing information; an internal thought leader and driver of thought leadership material for external audiences, e.g. white paper, webinar Project Director, responsible for strategic direction of projects, and meeting client objectives Conduct stakeholder interviews Key role in guiding team towards impactful recommendations and strategies Maintain communication with clients and the internal team throughout the course of the project Provide expert content knowledge on global healthcare systems, as well as disease-specific and technology-specific areas Proactively manage own and other's time across multiple simultaneous projects Position yourself as an expert and trusted advisor, ensuring deliverables add value Guiding and supporting the project manager on timelines, quality and profitability Encourage collaborative working across the Market Access team and the broader organisation Proactively communicate with colleagues at all levels to ensure mutual exchange of information Provide constructive feedback to colleagues on a project by project basis, identifying potential issues and offering solutions as they arise Utilise own knowledge and expertise to lead the induction and ongoing development of colleagues Expectation to take on the management of junior team members as appropriate Contribute to the leadership of the Market Access team Part of the senior leadership team Driving specific internal business initiatives Involved in setting and executing the direction of the team EXPERIENCE NEEDED: Market access solutions experience Experience in the pharmaceutical/healthcare sector an advantage Excellent knowledge of health systems and pricing and reimbursement processes, in particular in key countries in Europe Proven evidence of client engagement and business development success Highly developed project management skills Ability to work to tight and immoveable deadlines, e.g. proposal submissions Excellent organisational, writing and planning skill Additional language skills an advantage To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Our client is a leader in real world data and research solutions for healthcare and life sciences. They have innovative data & technology solutions. The company is part of a global group and they work with primary and secondary care data from the UK, USA and increasingly focus on EU. Research is conducted primarily using retrospective datasets and some prospective PRO data capture. The Head of Research sits inside the Delivery Team. The role has a remit including setting standards and best practice on data usage, owns and manages data applications whilst also owning data quality as part of leading an independent data function. The main objective of the Head of Research is the delivery and deployment of research projects, healthcare-related software and other products and services for the improvement of healthcare and access to medicines. The post holder will be part of the Senior Management Team. Responsibilities The Head of Research will design and implement studies on healthcare data (e.g. HES, CPRD, NCRAS oncology datasets etc.) including study methodology, statistical methods, data science techniques Attend client meetings to scope research projects, translating client needs for delivery Develop relationships with clients. Own client requirements, documenting and working with the delivery team to ensure adherence to the project scope, research principles, compliance and regulatory obligations The Head of Research will own and maintain relationships with data custodians Compose executive summaries, manuscripts, abstracts, and other communication materials to a quality that is publishable in peer-reviewed journals, or presentable in international conferences The Head of Research will evaluate existing risks and prediction of potential problems in research projects Develop new research methodologies, data sources, research outputs for the current and targeted clients Scout new opportunities on the horizon alongside the commercial department. Validation of Analyst team outputs as well as post project reviews. Manage all stages of data access applications Requirements Healthcare Analysis Knowledge of healthcare datasets, particularly in the UK (e.g. HES, CPRD, NCRAS, Oncology datasets etc.) Designing and delivery of research projects or creating technology and software in healthcare Statistical methodology and study design (e.g. inferential statistics, regression and modelling, demographics, prevalence and incidence etc.) Exposure data access applications including protocol writing, IRAS and ISAC applications Knowledge statistical techniques, especially in Microsoft Excel and other software such as R or Python Ideally degree qualified (Epidemiology/Medical Statistics/Public Health or other degree involving numerical analysis and/or health research) Desirable Working with clients in the pharmaceutical or medical device industry Health economics, health technology assessment Agile methodology and Business Transformation skills (Six Sigma, Lean processes) Machine Learning Techniques To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Our client is part of a group of global medical device companies. The brand specialise in sterile single-use surgical instruments, priding themselves on developing new and innovative products that are used for a variety of therapy areas. Reporting to the Head of Regulatory Affairs and based in Swansea there is some flexible working on offer if required for the chosen candidate. Role: The Regulatory Affairs Manager will be responsible for management of a team of technical file writers who share responsibility for all technical files for the site. Co-ordinate work undertaken by other specialists, clinical writer (s) and biocompatibility consultant etc. Act as the on-site expert on all regulatory matters, providing advise, guidance to QA, Manufacturing and other managers Create and maintain technical files to MDD requirements The Regulatory Affairs Manager will update Technical files to MDR Create and maintain technical documentation to US FDA requirements when needed Update Technical files to meet new products/modifications updates to technical documentation and supplier changes Oversee overseas registrations of products Review of and approve documentation and document change orders Assist in preparing responses to regulatory authorities' Write supplier agreements The Regulatory Affairs Manager will also be responsible for the RA plans for the design and development teams to support Global markets Assist and ensure devices are registered in EU/FDA and UK MHRA databases Stay abreast of regulatory procedures and changes in regulatory climate Support external regulatory agency audits, providing regulatory input to minimize potential for findings of non-compliance and addressing any issues arising. Qualifications & Skills: Ideally degree level education or practical experience in Regulatory Affairs Medical devices to MDD/MDR standard EU Medical Device regulations, harmonised standards and associated non-harmonised standards, Working Knowledge of US FDA requirements Knowledge of MDSAP desirable but not essential To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Our client is a leader in real world data and research solutions for healthcare and life sciences. They have innovative data & technology solutions. They serve customers across the drug lifecycle e.g. clinical trials, pharmacovigilance, HEOR and commercial. The company is part of a global group and work in the EMR division - they work with primary and secondary care data from the UK, USA and increa...... click apply for full job details

Our client is a leader in real world data and research solutions for healthcare and life sciences. They have innovative data & technology solutions. The company is part of a global group and they work with primary and secondary care data from the UK, USA and increasingly focus on EU. Research is conducted primarily using retrospective datasets and some prospective PRO data capture...... click apply for full job details

Our client is part of a group of global medical device companies. The brand specialise in sterile single-use surgical instruments, priding themselves on developing new and innovative products that are used for a variety of therapy areas. Reporting to the Head of Regulatory Affairs and based in Swansea there is some flexible working on offer if required for the chosen candidate...... click apply for full job details

Role Overview We are currently looking for a Senior QC Materials Analyst to join a growing biotechnology company based in South West London. As the Senior QC Materials Analyst you will work in the quality control department and you will be responsible for working with raw materials and establishing raw materials policy, flow strategy and processes. Duties and Responsibilities You will lead the sampling and testing of raw materials. You will work with programme management, quality, supply chain, development and manufacturing to meet deliverables and deadlines. As the Senior QC Materials Analyst you will be responsible for writing appropriate documentation such as materials policies, ensuring compliance and safety before releasing them. You will define management and flow strategies of product intermediates, raw materials, standards and consumables. You will support out of specification investigations, deviations, change controls related to raw materials. As the Senior QC Materials Analyst maintaining calibration, qualification and validation of material testing equipment will be among your duties. Education and Experience MSc or BSc in a relevant Scientific discipline and a number of years of industry experience working in QC including extensive experience with raw materials. Proven industry experience working in a GMP laboratory in a pharmaceutical or biotechnology/biopharma company is essential to your application. Proven experience with reagent preparation and material handling is essential for this position. To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales

Qualified Person (QP) - Pharmaceuticals Based in S. Yorkshire, you will be reporting to the Lead QP you will be taking a very hands on role in Batch Release duties, giving direct operational support to the manufacturing team (at all levels) and regulatory function as well as assisting with the QMS development and Batch Packaging Record generation. This is a family-feel Pharmaceuticals company, offering a generous salary and a great work-life balance. Qualified Person (QP) Requirements: Eligible to act as a Qualified Person as defined in EU directive 2001/83/EC for human medicines (or The Human Medicines regulations 2012, statutory instrument 2012 number 1916, part 3, regulation 41). Experience in high volume batch release Experience with marketing authorisation and variation submissions/categories. Experience in non-conformance reporting, systems and investigation tools as well as defining suitable CAPA Ability to complete risk assessments and concise yet technical reports Confidence in completing audits (internal and external), from planning through to writing the reports and reviewing CAPA. A working knowledge of GDP regulations and Brexit impacts If this Qualified Person (QP) opportunity in S. Yorkshire looks like it could be the next step in your Pharmaceuticals career, please get in touch ASAP ! To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales