At a Glance
- Tasks: Distribute safety reports and maintain trackers while collaborating with clinical teams.
- Company: Join Medpace, a leading company in clinical research based in Stirling.
- Benefits: Full-time position with competitive salary and opportunities for growth.
- Other info: Ideal for detail-oriented individuals passionate about healthcare.
- Why this job: Make a difference in patient safety and work in a dynamic environment.
- Qualifications: Bachelor's degree and 1 year of clinical trial safety experience required.
The predicted salary is between 50000 - 60000 £ per year.
Medpace, Inc. in Stirling, Scotland, is seeking a full-time Clinical Safety Coordinator to join our pharmacovigilance team.
The role focuses on distributing safety reports, maintaining trackers, and ensuring timely notifications while collaborating with Clinical Operations and Regulatory Submissions teams.
Ideal candidates have a Bachelor of Science and at least 1 year of clinical trial safety experience, with strong attention to detail and working knowledge of GCP guidelines.
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Pharmacovigilance Safety Coordinator in Stirling employer: Medpace, Inc.
Medpace, Inc. is an excellent employer for those seeking a dynamic role as a Feasibility Data Visualization Analyst in London. With a flexible work environment, competitive compensation, and a strong focus on structured career development, employees are empowered to grow and thrive while collaborating closely with clinical operations and medical teams to enhance data strategies. This supportive culture fosters innovation and meaningful contributions to clinical research.
