Clinical Research Jobs at Gilead UK
This Clinical Research Jobs opportunity with Gilead offers experienced life science professionals the chance to lead impactful global studies that address some of the world’s most serious diseases. Based in the UK, this role is ideal for candidates seeking senior clinical trials jobs that combine leadership, innovation, and meaningful patient outcomes—making it a strong job opportunity for life science graduates and experienced professionals alike.
About the Company
Gilead Sciences is a global biopharmaceutical leader committed to discovering, developing, and delivering innovative therapies for life-threatening diseases. With a strong presence in Clinical Research Jobs, Gilead leads global clinical trials jobs across multiple therapeutic areas while fostering a culture of inclusion, leadership development, and scientific excellence throughout the Jobs in UK market and beyond.
Clinical Research Job Details:
- Job Title: Clinical Trials Manager
- Company: Gilead Sciences
- Function: Clinical Operations
- Location: United Kingdom – Uxbridge
- Work Type: Full-time
- Work Arrangement: Onsite (Hybrid Eligible)
- Posted: Today
- Job Requisition ID: R0050151
Position Overview
Clinical Operations is responsible for the worldwide execution of Phase I–IV clinical trials across all Gilead therapeutic areas. The Clinical Trials Manager supports the delivery of high-quality clinical data in compliance with SOPs, company policies, and global regulatory requirements.
In this role, you will manage assigned geographic regions or components of clinical studies—typically Phase I or smaller studies—and contribute to broader strategic initiatives.
Key Responsibilities
- Manage all components of small clinical studies, including Phase I trials
- Support or lead CRO and vendor selection and manage related deliverables
- Serve as the primary operational contact for assigned studies
- Oversee site evaluation, initiation, monitoring, and close-out activities (directly or via CROs)
- Define study logistics and develop clinical study plans
- Manage study timelines, documentation, and communications
- Lead and participate in cross-functional project meetings and conference calls
- Contribute to SOP development, special projects, and process improvement initiatives
- Provide input into protocols, CRFs, informed consent forms, study plans, and presentations
- Ensure CRO and site compliance with protocols, SOPs, monitoring plans, and regulatory requirements
- Present at internal and external meetings as needed (e.g., investigator meetings)
- Lead or support preparation of safety, interim, and final study reports
- Identify operational risks and collaborate on mitigation strategies
- Assist in training and mentoring less experienced colleagues
- Ensure all work complies with company policies and regulatory requirements
Minimum Education & Experience
- PhD, MS, BS with relevant clinical or life sciences experience
- Multiple years of clinical or related life sciences experience
- Experience leading or managing less complex clinical studies and project teams
- Experience managing external vendors
- Meets requirements for Senior Clinical Trial Management Associate (Senior CTMA), Grade 26, with demonstrated proficiency
Knowledge, Skills & Competencies For Clinical Research Job
- Fast learner with adaptability to changing priorities
- Ability to manage full-cycle clinical studies from start-up through close-out
- Advanced knowledge of study management best practices and tools
- Strong understanding of clinical protocols and their practical application
- Thorough knowledge of:
- FDA, EMA, and applicable national regulations
- ICH guidelines
- Good Clinical Practice (GCP)
- Familiarity with medical and scientific terminology
- Clear, concise communication skills
- Ability to work effectively in a highly matrixed, team-oriented environment
- Ability to manage multiple tasks simultaneously
- Willingness to travel when required
