Our Safety activities are growing rapidly, and we are currently seeking a full‑time, Clinical Safety Coordinator to join our team in Stirling, Scotland. This position plays a key role in the pharmacovigilance process at Medpace, working in a team to accomplish tasks and projects that are instrumental to the company’s success.
If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities
- Responsible for the distribution of safety reports to regulatory authorities.
- Create and maintain project‑related trackers and status reports.
- Distribute and track safety‑related notifications.
- Conduct quality control reviews of departmental documents.
- Regular interaction with other internal departments globally and locally, such as Clinical Operations, Data Management and Regulatory Submissions.
- Perform other tasks as needed.
Qualifications
- Educated to degree level, Bachelor of Science.
- 1+ years clinical trial safety experience.
- Strong attention to detail.
- Comprehensive understanding of Microsoft Office suite.
- Demonstrate fundamental knowledge of Good Clinical Practice (GCP) guidelines and medical terminology (preferred, but not mandatory).
- Knowledge of Electronic Data Capture (EDC) systems and other clinical databases (preferred, but not mandatory).
- Knowledge of applicable safety reporting guidelines (preferred, but not mandatory).
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
What To Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Clinical Safety Coordinator in Stirling employer: Medpace
Join our dynamic Clinical Operations team in London, where we prioritise employee growth and foster a collaborative work culture. As a Clinical Trial Site Relationship Coordinator, you'll benefit from ongoing professional development opportunities while working in a vibrant environment that values strategic relationships and innovative solutions in clinical research. Enjoy the unique advantage of reduced travel while making a meaningful impact in the field of clinical trials.
