ICON - EMEA

Biostatistician I Swansea Office Based Recruitment commencing from January 2023 onwards! We are looking to grow our Biostatistics team in Swansea with an Academy Program starting in September 2023. Our Swansea Office is home to multiple graduate schemes and has a strong record of producing fantastic experts in their respective fields. This also sets it apart as being a great social environment and its modern city centre, waterfront building makes it a brilliant place to work At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. The role: ICON's Biostatistics Academy is our specially designed program to kickstart your career as a Biostatistician in the Clinical Trials industry. We provide you with everything you need to know about the industry and your role within it through a mixture of instructor-led training, practical experience and mentoring. You will gain technical skills such as Statistical Programming in SAS and creating Statistical Analysis Plans, as well as skills for life such as communication and project management. A dedicated Training Manager will deliver the program and be available for providing support. In return, we are looking for your enthusiasm, inquisitive mind and fresh perspective. Under the supervision of senior biostatisticians, this position is responsible for statistical aspects of clinical research projects. Project responsibilities include: Contributes to the development of statistical analysis plans, including creation of table, figure and listing (TFL) shells. Writes programs to select, manipulate and analyse data, and assists senior biostatistician in interpreting results of these analyses. Prepares statistical summary reports and writes the statistical methods sections of integrated study reports under the supervision of senior biostatisticians. Assists senior biostatistician in statistical aspects of case report form (CRF) design. Establishes and maintains effective working relationships with ICON project team members, including data management personnel, statistical programmers, and clinical research colleagues. Performs additional duties as assigned. You will need: Master's degree or above in Statistics or related field Excellent verbal and written communication skills Ability to work as part of a team Strong attention to detail Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

Project Manager At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. Summary: The Project Manager (PM) role in Accellacare is responsible for ensuring the successful delivery of projects from project kick-off to finish. The PM manages the delivery of assigned projects with the support of other team members. As required, the PM will manage and support other ad-hoc projects/ initiatives in Clinical Operations. Responsibilities: • Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance. • As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. Sponsor Facing • To demonstrate excellent communication skills • To demonstrate excellent presentation skills • To develop and maintain excellent client relationships where required • To manage project related issues during the lifecycle of all assigned projects • To develop and maintain excellent relationships with ICON, Sponsor and third party teams . • Facilitate post-project evaluations e.g. project closeout, action and assign ownership of any resulting actions • To collaborate with key stakeholders to ensure up-front pre-requisite items are in place to support the project (e.g. client deliverables, customer requirements/etc.) • To monitor client satisfaction trends together on a monthly basis • To review and manage any client related issues with study performance to find solutions to address any possible conflicts • To represent Accellacare to the highest standard at all client meetings • Client relationship management, build and maintain relationship with client through project delivery . Project Management • To demonstrate a strong ability to work as part of a team • To manage and motivate a production team to deliver projects on time and within budget • To feedback on team and team member performance • To facilitate process improvements • To ensure provision of project source material and project processess. • To ensure changes in scope are appropriately managed • Conduct project related meetings e.g. handover meeting, kick-off meeting (via teleconference or face-to-face) • Complete and communicate Project Plan Complete Risk assessments & demonstrate and apply risk and issue mitigation strategies • Set up all relevant Project Meetings • Provide all project related information from Sponsor to team Report KPIs on a weekly basis • Deal with any project progress delays promptly • Drive continuous improvement with the production team • Travel (approximately 20%) domestic and/or international as required • Other duties as assigned. Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. We have an incredible opportunity for an expert Clinical Data Programming Lead to join the team. This role can be office based or remote working within EMEA. Highlights of Key Responsibilities: Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets. Build SDTM data set specifications per specified study requirements. Program data sets per specification, and validate data sets per the formal, documented CC process Build data programming specifications per specified study requirements Program clinical data programs per specification Validate clinical data programs per the formal, documented CC process. Execute programs and generate clinical data outputs to according to study/client requirements. Review and quality assure CRF annotations produced by other programmers. Participate in testing of clinical data system upgrades and documenting of test scripts when required. Lead programming and validation activities across a single project, ensuring that timelines are met and deliverables are of sufficient quality. To succeed you will need 4+ years of experience clinical data programming and delivery Demonstrated ability to produce CDISC and sponsor defined clinical data deliverables Experience building SDTM data set specifications Experience annotating CRFs in accordance with CDISC or sponsor specific guidelines Successfully handle multiple tasks and timelines. Team player with strong verbal and written communication skills Advanced knowledge of the clinical data programming development life cycle Bachelor's degree in information systems, science or related discipline Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

Oncacare (UK) Limited - Global Oncology Site Network Role: Proposals Manager Job Type: Full time Location: London, UK Working arrangement: Hybrid Travel Requirements: Occasional domestic and international travel Introduction Are you looking for an outstanding opportunity to develop your career with ICON s leading edge Global Commercial Oncology Site Network which is growing fast? Oncacare, in partnership with ICON plc, is an Oncology Site Network which concentrates on developing high performing sites by accelerating start-up timelines and focussing on high level of patient enrolment with strong attention to data and quality standards. These qualities are what our Sponsors look for in a leading Oncology Site Network and you can be part of our success story. We are growing our international footprint and you can play a part in our expansion and be involved in the future of oncology treatments across the globe. Oncacare is passionate about transforming cancer research to advance new treatments. Our strong capabilities enable us to bring together Patients, Sites and Pharmaceutical organisations to present a unique solution to the cancer trials industry. The Oncacare global site network provides opportunities for patients and oncologists to advance the development of cancer treatments more quickly and efficiently. We are a change agent for cancer clinical research. Quality, Patient Centricity, Delivery, Staff and Prospects are our principal values at Oncacare. They are fundamental in shaping the way in which we work and map out our future. By working to these values, we can achieve our objectives and ensure our teams are fully engaged, patients are enrolled and trial results are consistently realised for our customers. Main Responsibilities: Deliver high quality customer-focused proposals and budgets for new business opportunities within a given timeframe Evaluate and understand client requirements for incoming Request for Proposals (RFPs) Manage and oversee the preparation, review and submission of proposals and budgets for new business opportunities within given timeframe Manage and lead the proposal generation process including attending the proposal kick off, resource, clinical strategy and other opportunity specific meetings as required Ensure that the appropriate personnel including Senior Management, Operations and Sales are involved as required throughout the proposal generation process Attend bid defence and other client meetings as a support role as required Ensure Senior Management are apprised of the status of proposal preparation and elevate any issues or concerns Recruit, train and mentor Feasibility and Proposals Associates as appropriate Develop a training plan for each Proposal Development Associate as required Contribute to the development of Standard Operating Procedures (SOPs) Contribute to the development of processes and tools to improve the accuracy and quality of proposals and contracts Assist with continuous departmental process improvements and participate in special projects periodically assigned, in addition to day-to-day duties Comply with Oncacare s administrative, training and human resources policies To be successful you will need (Qualifications and Skills): Bachelor's degree or equivalent Prior experience successfully performing the role of a proposal developer (a minimum of 4 years' experience) Self-starter and able to function in a high-paced, dynamic environment Must be able to work independently, be highly motivated and a strong team player Ability to work under pressure to meet tight deadlines while maintaining accuracy and attention to detail Ability to evaluate RFPs and identify critical issues and questions Good understanding of industry cost drivers and budget algorithms Excellent numeracy, communication and organizational skills Excellent working knowledge of Microsoft Excel and Microsoft Word Fluency in English and excellent written English skills are essential Ability and willingness to travel at least 10% of the time If you are interested in applying, please provide a one sided supporting statement (A4 page) with a brief summary of how you meet the requirements of the role along with your salary expectations. Why join us? Ongoing development is vital to us, and as a Proposals and Feasibility Manager at Oncacare you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success. Benefits: Discretionary Bonus scheme Company pension Cycle to work scheme Life insurance Private dental insurance Private medical insurance Sick pay We are an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. Are you a current ICON Employee? Please click here to apply: link

At ICON, it s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our Own It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That s our vision. We re driven by it. And we need talented people who share it. If you re as driven as we are, join us. You ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you ll be helping shape an industry. The role: ICON are currently recruiting for a Sales Analyst based in either Dublin, Swansea or Reading. This is an exciting opportunity for either a recent graduate or someone who is looking for a change in direction to start their career in sales! Key responsibilities include: Enter and update Accounts, Contacts, Leads, and Opportunities records Load tradeshow and other Lead lists Transfer ownership of records Identify duplicates and de-duplicate records using automated tools Identify and correct data gaps and discrepancies Research larger companies and update Account hierarchies Research company pipelines and identify sales-ready Leads Run regular reports to identify data discrepancies across the system Maintain large Contacts directory: Run routine jobs to cleanse and update records Perform research and use third-party tools to identify discrepancies and update records Update training documentation and other support materials Build a range of system reports and provide to targeted groups/personnel Publish routine Campaign reports for Sales and Marketing team Coordinate training for new users You will have: Knowledge of CRM systems, and some experience with cloud computing technology. Some knowledge of 3rd party applications. Uses strong technical background to maintain the highest level of data quality in SalesForce. Benefits of working in ICON: Our success depends on the quality of our people. That s why we ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link

At ICON, it s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our Own It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That s our vision. We re driven by it. And we need talented people who share it. If you re as driven as we are, join us. You ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you ll be helping shape an industry. The Role: We are looking for a Senior Clinical Supplies Manager to provides scientific, technical and regulatory support to projects that have significant Pharmaceutical Supply Management, Chemistry, Manufacturing and Control (CMC) activities associated with them and to act as the lead on appropriate project teams. You will be managing global pharmaceutical supply for all phases and pharmaceutical development activities on-going at contract facilities with respect to technical, quality, timing and cost standpoint on behalf of our clients. Oversee labelling, packaging and distribution activities of CMO including review and approval of labelling / packaging records and distribution plans. Oversee recall, returns and destruction activities, as appropriate Oversee the procurement of marketed drug product, such as comparators performed by an approved vendor and ensuring together with GRA / SSU that all study specific regulatory requirements are met. Perform Batch Record Review and Approval, as applicable. Manage temperature deviation, product complaints and recalls, as delegated by the client. Gap analysis of processes relating to pharmaceutical supplies for applicable project teams. Participates in the discussions of objectives and scope of prospective projects with potential clients. Maintain confidentiality of management information as appropriate. Liaise with other managers to improve the effectiveness of the organisation Travel (approximately 10%) domestic and/or international. To undertake other reasonably related duties as may be assigned from time to time. Benefits of Working in ICON: Our success depends on the quality of our people. That s why we ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link

Senior Feasibility Associate Location: UK - Remote-working At ICON, it s our people that set us apart. As a global provider of drug development solutions, our work is serious business. But that doesn t mean you can t have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry! Are you one of them? At ICON, we have an incredible opportunity for a Feasibility Associate to join our UK team. The Role Summary: The Feasibility Associate will be supporting securing the right trials for Accellacare Research sites to be successful with randomization activity and revenue generation. This role will be responsible for trial analysis and centralized feasibility processes for the Accellacare Research network. Responsibilities: Execute effective, accurate network feasibility and deliver project proposals that maximize secured randomization opportunities for Accellacare Research within assigned therapeutic areas Communication skills to be able to collaborate with the Communications and Operations team to ensure trial enrollment projections are realistic and optimized. Conduct timely centralized follow up and provide excellent communication back to Accellacare Research sites regarding project status. Entry of feasibility and maintenance of key data into our CTMS systems that supports predictability, randomizations, forecasting, and other key performance measures within assigned therapeutic areas. Ensure proficiency and knowledge of therapeutic area expectations. Create files and upload appropriate documents to Clinical Conductor Meeting/exceeding goals set for randomizations secured by assigned therapeutic areas. Ensure trials are well matched as evidenced by meeting and exceeding contracted goal per assigned therapeutic areas. Ensure predictability of performance targets are met/exceeded within assigned therapeutic areas. Collaborate with Accellacare teams involved in the Study Start-Up process. Comply with all federal and local regulatory requirements as well as company policies. Travel to other sites within the network may be required. What you will need: Bachelor s Degree in medicine, science or your equivalent working experience You should be a confident communicator, with strong client management skills and strong decision-making skills Why join us? Other than working with an outstanding team of ambitious people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage. We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career. Ongoing development is vital to us, and as a Feasibility Associate, you will have the opportunity to progress your career, with the potential to move into other related areas to improve your skillset. Our benefits package is competitive, our scope is international and we sincerely care about our people and their success. ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment. EOE race/colour/religion/sex/sexual orientation/gender identity/disability/vet/national origin Are you a current ICON Employee? Please click here to apply: link

At ICON, it s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our Own It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That s our vision. We re driven by it. And we need talented people who share it. If you re as driven as we are, join us. You ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you ll be helping shape an industry. Principal Biostatistician Position Summary This position will be accountable for the leadership of the Biostatistics and Programming activities of a program of studies of moderate complexity and/or of high value with high impact for the organization. Also responsible for planning, monitoring, organizing and reviewing activities of biostatisticians and programmers working on the assigned program of studies, ensuring individual studies and the overall program of studies and integrated analyses are delivered on time, on budget to required quality. Accountabilities also include maintenance of consistency across studies. Responsibilities: • Accountable for leading Biostatistics and Programming activities for a program of studies of high complexity and/or of high value with high impact. • Bio statistical input into the design of the program, Protocol input such as study design, sample size calculations and patient randomization schemes and Statistical aspects of case report form design • Review project database structures, edit checks and data management coding conventions • Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports • Statistical analysis, Interpretation of data and reporting of results. • Writing of the statistical methods sections of integrated study reports. Reviews draft integrated study reports. • Supports responses to regulatory questions on the design of the program, and any labelling claims following submission • Participates in presentations at client and investigator meetings. • Preparation of biostatistics input to ICON research proposals, and participates in proposal defense meetings and makes presentations at marketing meetings with prospective client. • Ongoing coaching and mentorship of team members. Key Requirements: • M.S. degree in statistics, biostatistics, or related field with minimum of 9 years of relevant experience (at least 8 of which must be in the pharmaceutical industry); or Ph.D. in statistics, biostatistics, or related field with minimum of 7 years of relevant experience (at least 6 of which must be in the pharmaceutical industry). • Experience with oncology is required • In-depth knowledge of study designs, and statistical analysis applications in one or more therapeutic areas. • Excellent verbal and written communication skills as well as interpersonal and project management skills • Excellent knowledge of a wide variety of principles, theories and concepts in statistics and experimental design; must be able to apply them to the development and analysis of clinical trials • Excellent knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages, including SAS are a must. • Experience leading a regulatory submission • Must be able to translate clients needs into statistical practice and educate clients in the use of statistics. Benefits of Working in ICON: Our success depends on the quality of our people. That s why we ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link

At ICON, it s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our Own It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That s our vision. We re driven by it. And we need talented people who share it. If you re as driven as we are, join us. You ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you ll be helping shape an industry. Study Start Up Associate II As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices. The Role • To review and negotiate clinical site investigator contracts and budgets. • Stay connected with Investigative sites, sponsors and internal personnel regarding the status of contracts and contract-related documents • Prepare and coordinate preparation of contractual documents and correspondence • Facilitate the indemnification process between the study sponsor and the site. • Function as the internal consultant on study budgets (investigator payments, develop and update training documentation and conduct group training as necessary, mentor and train new and junior personnel in the SSU department, and act as consultant on the Investigator Contract and Budget development process from origination through execution). What you need • A bachelor s degree in Paralegal Studies, Juris Doctor (law) degree, or related experience is preferred • SSU experience is desirable but not required. • Experience in a clinical research environment with specific experience in study contracts review and budget negotiation or in related field such as where contract or legal document review is a primary part of you role. Benefits of Working in ICON: Our success depends on the quality of our people. That s why we ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link

At ICON, it s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our Own It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That s our vision. We re driven by it. And we need talented people who share it. If you re as driven as we are, join us. You ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you ll be helping shape an industry. As a Study Support Assistant (SSA), you will play a key role in independently assisting the team to ensure the most effective and efficient study start up, by providing administrative and tracking support. The Role • Supporting the Study Start up Associate with tasks including; tracking, filling, collating and verifying, for completeness, submission documentation for submission to the Regulatory/Competent Authority (CA)/Ethics Committee(EC) and other relevant authorities and helping with the translation of these documents • Looking after the submission progress tracking by updating the relevant ICON/Sponsor tracking system. • Be proficient with ICON/Sponsor Clinical Trial Management System (CTMS). • Setting, up, coordinate and maintain department electronic filing systems. • Coordinate and attend meetings as requested and assist in the production of slides, overheads etc as needed • Assisting in the co-ordination of payments to CA/EC and other relevant authorities and be familiar with ICH GCP and ICON SOPs What you need • The successful candidate will have a high school diploma, or local equivalent with good interpersonal skills and the ability to handle multiple tasks with meticulous attention to detail • Research or Healthcare related academic or work experience would be preferable but not essential • You will possess excellent written and verbal communication in English Benefits of Working in ICON: Our success depends on the quality of our people. That s why we ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link

ICON plc is a world - leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the cen tre of all that we do, we help t o accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the drivin g force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. Senior Clinical Research Associate & CRA II opportunities Location: UK - wide The Role Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness Dependent on level of experience you may assist in training and mentoring less expert CRA s and/or lead CRA s working on international projects To be successful in the role you'll need: 2 years + of monitoring experience in phase I-III trials as a CRA Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data You will possess excellent written and verbal communication in English Ability to produce accurate work to tight deadlines within a pressurized environment You will be available to travel at least 60% of the time and should possess a valid driving license Benefits of Working in ICON : Our success depends on the knowledge, capabilities a nd quality of our people. That s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to p rovide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive poli cies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If , because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link

ICON: Clinical Research Coordinator - Assistant Location: South London At ICON, it s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our Own It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That s our vision. We re driven by it. And we need talented people who share it. If you re as driven as we are, join us. You ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you ll be helping shape an industry. Summary: This position is accountable for supporting the Clinical Research Coordinators for both clinical and clerical assigned tasks in an accurate and timely manner in accordance with the SOP s, COG s, and ICH guidelines. Responsibilities: • Assisting Clinical Research Coordinators with patient visits, documentation, CRF completion, data queries and monitor visits. • Performing technical requirements of study protocols, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or coordinator. • Assisting in the laboratory or with other laboratory duties such as performing quality assurance review, restocking of supplies and processing of specimens. • Performing consult visits as needed. • Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment. • Assisting the Clinical Research Coordinator or other staff members with creating and copying patient files for study closeout procedures. • Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor. • Addresses all queries or data clarifications within 48 hours of receipt. • Typing memos, letters, recruitment tools, progress notes and various documents. • Filing labs and correspondence. • Performing various errands to pick up dry ice, supplies, samples, physician signatures and storage boxes, etc. • Assisting Clinical Research Coordinators or other staff members as determined by the needs and priorities of the research organization, and as time and abilities permit. • Assisting with answering the telephones, making appointment reminder calls and initial phone screening. • Travel: Travel to other sites within the network may be required to support increases in workload and, or studies/projects as needed. Benefits of Working in ICON: Our success depends on the quality of our people. That s why we ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Are you a current ICON Employee? Please click here to apply: link