Fsp Jobs In UK - 712 Job Positions Available

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll do meaningful work that has a positive impact on a global scale. Through our PPD clinical research portfolio, we help customers bring our Mission

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. The CDM ensures, from a data management perspective,

The Senior Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Location: Home-based, UK or Sweden At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission

As a Principal Biostatistician, you will provide end‑to‑end statistical leadership and integration support across Phase II and Phase III studies, working closely with cross‑functional stakeholders in a fast‑paced, global environment. Key Responsibilities • Provide Principal‑level Biostatistics

Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

Who Are You? An experienced R/AI Developer with a passion for clinical development and analysis, adept at utilizing advanced programming and data science methods, you will lead development activities to improve clinical studies. You are excited

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as a Site Contract Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs,

Principal Epidemiologist, Internal Medicine, Inflammation & Immunology (FSP Sponsor Dedicated) Location: Remote, candidates should preferably be based in Spain, Portugal or UK (other EU locations may be considered). Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Manager Strategic Feasibility – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750

The EDC Clinical Trial Designer will create high quality data collection tools for new clinical trials and facilitate activities related to the design, development, documentation, testing and implementation of clinical eCRF databases. Design of eCRF forms

This position is responsible for encoding terms reported as adverse events and medical history as well as prior and concomitant medications using industry accepted dictionaries such as MedDRA and WHOdrug. Summary of the Essential Functions of

Who Are You? An experienced RWE Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead studies across your region. You are excited and enthusiastic, motivate your teams

Position Summary: Quotient is seeking a Senior Engineer in our Data Infrastructure team to design and evolve our cloud, data and AI infrastructure underpinning our genomics-first drug discovery platform. Working within the Data Infrastructure team, you