Clinical Safety Coordinator
On-siteStirling, Scotland, United Kingdom
Stirling, Scotland, United KingdomOn-siteFull TimeBachelors DegreeLarge
Full TimeBachelors DegreeLarge
Job Summary
Distribute safety reports to regulatory authorities and track safety-related notifications while creating and maintaining project-related trackers and status reports. Conduct quality control reviews of departmental documents and facilitate regular interactions with internal departments globally and locally, including Clinical Operations, Data Management, and Regulatory Submissions. Perform other tasks as needed to support the pharmacovigilance process within our growing safety activities team.
Required Qualifications
- Educated to degree level, Bachelor of Science
- 1+ years clinical trial safety experience
- Strong attention to detail
- Comprehensive understanding of Microsoft office suite
Desired Qualifications
- 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)
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.