Clinical Safety & PV Specialist

Medpace; Stirling; On-site; GBP 36,000 - 60,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits

Structured career paths

Company-sponsored events

Employee health and wellness

PTO

Job summary

Medpace is expanding its European Pharmacovigilance activities and seeks motivated individuals to join our Clinical Safety team in Stirling, United Kingdom. You will work alongside Medical Monitors, QA, and Trial Management to ensure safety reporting and compliance across global trials.

Responsibilities include SAE processing, safety narratives, database QC, safety documents, and participation in sponsor meetings.

Qualifications

• Minimum Bachelor’s life science degree.
• 2+ years of Clinical Trial Pharmacovigilance experience.
• Working knowledge of Safety Databases (Argus is desirable).
• Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines.
• Exposure to working on global trials as part of a multidisciplinary team.

Responsibilities

• Collect, process, and track SAE reports.
• Generate safety narratives and queries.
• Safety Database data entry.
• Perform quality control of safety cases.
• Generate Investigator Safety Letters.
• SAE reconciliation between safety database and clinical database.
• TMF uploads and quality control review.
• Preparation of clinical safety documents (e.g., safety management plan, periodic safety reports).
• Attend internal and external meetings (sponsor TCs and audits/inspections).
• Lead clinical trial projects to meet client deliverables and provide oversight.

Skills

Pharmacovigilance experience

GCP knowledge

Education

Bachelor’s degree in life science

Tools

Argus

Job description

Medpace is expanding its European Pharmacovigilance activities and seeks motivated individuals to join our Clinical Safety team in Stirling, United Kingdom. You will work alongside Medical Monitors, QA, and Trial Management to ensure safety reporting and compliance across global trials.

Responsibilities include SAE processing, safety narratives, database QC, safety documents, and participation in sponsor meetings.