Pharmacovigilance Safety Specialist — Clinical Trials

Medpace; Stirling; On-site; GBP 40,000 - 60,000; Full time

Job summary

A clinical contract research organization is seeking a Clinical Safety Coordinator in Stirling. In this role, you will collect and track serious adverse events, generate safety narratives, and ensure compliance throughout clinical trials, working within a multidisciplinary team. The ideal candidate has a Bachelor's degree in life sciences and 2+ years in Clinical Trial Pharmacovigilance. Medpace offers a competitive compensation package and professional growth opportunities in a flexible work environment.

Benefits

Flexible work environment

Competitive compensation and benefits package

Structured career paths

Company-sponsored employee appreciation events

Qualifications

• 2+ years of Clinical Trial Pharmacovigilance experience.
• Minimum Bachelor’s life science degree.
• Working knowledge of Safety Databases.

Responsibilities

• Collect and track serious adverse event (SAE) reports.
• Generate safety narratives and perform quality control.
• Lead clinical trial projects and ensure compliance.

Skills

Clinical Trial Pharmacovigilance experience

Knowledge of Safety Databases

Medical terminology

Good Clinical Practice (GCP) Guidelines

Global trial exposure

Education

Bachelor’s degree in life sciences

Tools

Argus

Job description

A clinical contract research organization is seeking a Clinical Safety Coordinator in Stirling. In this role, you will collect and track serious adverse events, generate safety narratives, and ensure compliance throughout clinical trials, working within a multidisciplinary team. The ideal candidate has a Bachelor's degree in life sciences and 2+ years in Clinical Trial Pharmacovigilance. Medpace offers a competitive compensation package and professional growth opportunities in a flexible work environment.