Clinical Research Jobs in London, UK | Medpace Hiring Life Science GraduatesÂ
Step into a high-impact position at the center of global drug safety. These Clinical Research Jobs opportunity gives life science professionals the chance to contribute to life-changing clinical development while advancing their career in a rapidly growing pharmacovigilance environment. Ideal for candidates pursuing clinical trial jobs, this role blends scientific expertise, global collaboration, and meaningful work that supports safer, more effective therapies for patients worldwide.
About the Company
Medpace is a global, full-service clinical contract research organization (CRO) dedicated to accelerating the development of safe and effective medical therapies. With more than 5,000 employees across 40+ countries, Medpace delivers scientific expertise, regulatory guidance, and operational excellence across therapeutic areas including oncology, cardiology, CNS, infectious disease, and metabolic disorders. Widely recognized for quality and reliability, jobs at Medpace provide structured career paths, competitive benefits, and meaningful opportunities that empower professionals to contribute to global health advancements.
Job Details:
- Job Title: Clinical Safety Coordinator – Pharmacovigilance / Drug Safety
- Location: London, United Kingdom
- Department: Clinical Safety
- Job ID: 10508
Job Summary
Medpace’s European Pharmacovigilance (PV) operations are expanding rapidly, and we are seeking motivated individuals to join our Clinical Safety team in London. In this role, you will collaborate with Medical Monitors, Quality Assurance, Clinical Trial Management, and cross-functional teams to support the safety oversight of life-changing medicines. This is an excellent opportunity to grow your skills and work on impactful clinical development projects.
Responsibilities in Clinical Research Jobs
- Collect, process, and track Serious Adverse Event (SAE) reports
- Generate safety narratives and queries
- Perform Safety Database data entry
- Conduct quality control (QC) of safety cases
- Generate Investigator Safety Letters
- Perform SAE reconciliation between safety and clinical databases
- Upload and QC documents within the Trial Master File (TMF)
- Prepare clinical safety documents (e.g., Safety Management Plans, periodic safety reports, presentations)
- Attend internal/external meetings, including sponsor teleconferences, audits, and inspections
- Lead clinical trial projects, ensuring compliance and timely delivery of client requirements
Additional Responsibilities
- Develop and present materials for sponsor-facing meetings (e.g., Kick-Off Meetings, Investigator Meetings)
- Coordinate final medical review of study report narratives
- Draft adjudication materials (charters, reporting documents)
- Provide periodic safety summaries to the Data Manager, Clinical Trial Manager, and Medical Monitor
- Train new Clinical Safety Coordinators
- Coordinate safety responsibilities for aggregate reporting (data entry timelines, pending case tracking, collaboration with Medical Monitor and Regulatory Affairs)
Qualifications for Clinical Research Jobs
- Bachelor’s degree in a life science discipline (minimum)
- 2+ years of Clinical Trial Pharmacovigilance experience
- Working knowledge of safety databases (Argus preferred)
- Strong understanding of medical terminology, global safety reporting requirements, and Good Clinical Practice (GCP)
- Prior experience supporting global trials within multidisciplinary teams
Medpace PerksÂ
- Flexible work environment
- Competitive compensation and benefits
- Generous PTO packages
- Clear career pathways and professional development opportunities
- Company-sponsored appreciation events
- Employee health and wellness programs.
