Job Summary
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, not mandatory);
- Knowledge of Electronic Data Capture (EDC) systems and other clinical databases (preferred, not mandatory);
- Knowledge of applicable safety reporting guidelines (preferred, not mandatory).
Clinical 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.
