Clinical Trial Jobs at Medpace
Medpace is hiring a Clinical Safety Coordinator – Pharmacovigilance / Drug Safety to join its rapidly expanding European Clinical Safety team in Stirling, United Kingdom. The Clinical Trial Jobs at Medpace offer a dynamic opportunity to work across global clinical trials, supporting pharmacovigilance activities that directly contribute to the development of life-changing medicines. You will collaborate with Medical Monitors, Clinical Trial Managers, Quality Assurance, and Regulatory teams in a fast-paced CRO environment.
Job Details:
- Job Title: Clinical Safety Coordinator – Pharmacovigilance / Drug Safety
- Job ID: 10506
- Department: Clinical Safety
- Location: Stirling, United Kingdom
- Employment Type: Full-Time
- Industry: Clinical Research / Pharmacovigilance / Drug Safety
About the Company:
Medpace is a global, full-service Contract Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries and supports studies in oncology, cardiology, CNS, metabolic disease, endocrinology, anti-viral, and anti-infective therapies. With a strong scientific foundation and disciplined operational approach, Medpace is committed to accelerating the development of safe and effective medical therapeutics worldwide.
Educational Requirements:
-
Bachelor’s degree in Life Sciences or related field
Key Responsibilities of the Clinical Safety Coordinator:
- Collect, process, and track Serious Adverse Event (SAE) reports
- Perform safety database data entry and quality control of safety cases
- Generate safety narratives, queries, and Investigator Safety Letters
- Reconcile SAEs between safety and clinical databases in this Clinical Safety Coordinator Role.
- Prepare and review the Trial Master File (TMF) safety documentation
- Assist in the preparation of safety management plans, periodic safety reports, and presentations
- Attend sponsor meetings, audits, inspections, and internal safety discussions
- Lead clinical trial safety activities to ensure timely client deliverables and regulatory compliance
Skills Required for the Clinical Trial Jobs:
- 2+ years of experience in Clinical Trial Pharmacovigilance
- Strong working knowledge of global safety reporting requirements and GCP guidelines
- Hands-on experience with Safety Databases (Argus preferred)
- Advanced understanding of medical terminology
- Experience working on global, multi-center clinical trials
- Excellent communication, documentation, and organizational skills
- Ability to work effectively in cross-functional teams
Benefits of the Clinical Trial Jobs at Medpace:
- Flexible and supportive work environment
- Competitive salary and benefits package
- Generous paid time off (PTO)
- Structured career development pathways
- Employee health and wellness initiatives
- Company-sponsored appreciation and recognition events
- Opportunity to work on global clinical trials impacting patient lives
