Clinical Science Associate

Job Title:Clinical Research Associate LeadAbout the Role:IQVIA UK is seeking an experienced Clinical Research Associate Lead to strengthen our cFSP team. The successful candidate will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, and managing study sites to ensure compliance with Good Clinical Practice...

OverviewIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.About the RoleWe are looking for a skilled Clinical Research Associate to join our team in Argentina. As a CRA, you will be responsible for conducting site monitoring visits, administering protocol and related...

Based in the UK, ICON plc is a world-leading healthcare intelligence and clinical research organization.We are seeking a Clinical Research Associate to join our diverse team at ICON Plc. As a key member of our research department, you will oversee and coordinate clinical trials, ensuring compliance with regulations and collecting critical data.Key...

About the Role:IQVIA, Inc. is looking for a talented Clinical Research Associate to support its operations in the South West of England. As a CRA, you will be responsible for conducting site monitoring visits, managing study progress, and escalating quality issues. This role offers a range of opportunities for growth and development in a dynamic team...

About the RoleThis Senior Position offers an excellent opportunity for a seasoned data scientist to lead our clinical data science efforts. The ideal candidate will have extensive experience in applying data science methodologies to clinical research and development.In this role, you will be responsible for providing strategic direction and oversight for...

Job SummaryIQVIA UK is seeking experienced professionals to strengthen our cFSP (sponsor-dedicated) team. As a Clinical Research Associate Lead, you will play a vital role in ensuring the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.About UsIQVIA is a leading global...

We are seeking a skilled and detail-oriented Trial Support Specialist to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences, Pharma, and IT.**Job Summary:**The ideal candidate will have minimum 6 months of clinical research experience and possess strong organizational skills, effective time management, and excellent communication...

OverviewIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.Salary & BenefitsWe offer competitive salaries with a range of $80,000 - $110,000 per year, depending on experience. Our comprehensive benefits package includes health insurance, retirement savings plan, paid...

Career Opportunities: CK Group- Science, Clinical and Technical is seeking a talented Technical Operations Manager to join their team in Reading.About the JobThis is a contract-based position for 12 months, offering a unique opportunity to work with a global Consumer Healthcare company.As the Technical Operations Manager, you will lead technical materials...

Clinical Development AssociateWe are seeking a highly skilled Clinical Development Associate to join our team at ICON plc. In this role, you will be responsible for maintaining and expanding client relationships through clinical outcome assessment (COA) licensing and translation services.Key Responsibilities:Deliver high-quality customer service via the...

**Job Overview:**We are seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team at Lifelancer, a talent-hiring platform in Life Sciences.**Responsibilities:Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams with updating and maintaining clinical documents and systems, including the Trial...

Clinical Research Associate I Role OverviewCompany OverviewICON plc is a leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence.Salary and BenefitsWe offer a competitive salary of £45,000 - £55,000 per annum, depending on experience. In addition to your base salary, you...

We are seeking a highly skilled Clinical Trials Governance Specialist to join our team at IQVIA. This exciting role will focus on providing expert-level support in coding governance and associated processes, ensuring the highest level of accuracy and reproducibility in clinical study data coding.About the Role:This is a full-time position offering a...

We are seeking a Clinical Research Associate to support our client sites across the South West of England. As a member of our team, you will have the opportunity to work with a leading global provider of clinical research services and contribute to the success of our clients.Key ResponsibilitiesPerform site monitoring visits in accordance with contracted...

Job DescriptionWe are seeking an experienced Principal Clinical Data Science Lead to join our team at ICON plc. This role is a critical part of our Early Development Services (EDS) division, which provides early-phase clinical research and bioanalytical services to the pharmaceutical and biotechnology industries.The successful candidate will be responsible...

Job DescriptionThis Study Start-Up Associate Manager position plays a vital role in the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.You will be responsible for managing and maintaining comprehensive and accurate records of regulatory submissions,...

Company OverviewPharmiweb is a leading provider of innovative solutions for the pharmaceutical and biotechnology industries.Salary$120,000 - $150,000 per year, depending on experience and qualifications.Job DescriptionWe are seeking an experienced Clinical Trials Vendor Category Manager Imaging to join our team. The successful candidate will be responsible...

ResponsibilitiesThe successful candidate will be responsible for:Leading the design and implementation of advanced data science methodologies and statistical models to support clinical research and data analysis.Guiding a team of data scientists and analysts in the development and execution of data-driven strategies to optimize clinical trial design and...

Clinical Affairs Director (Multiple Sclerosis) is a leadership role requiring strategic planning, execution, and oversight of medical initiatives within the Multiple Sclerosis therapeutic area. Candidates with a background in medical affairs or HCPs transitioning into the pharmaceutical sector are encouraged to apply.Main Duties:Design and implement...

Job Overview:Clinical data programmers play a vital role in the development and commercialization of innovative medical treatments. As a Clinical Programmer (Data Visualization Expert) at IQVIA, you will be responsible for developing, testing, and validating clinical data programs and applications.Key Responsibilities:• Develop and test clinical data...