Medpace is seeking a full-time Clinical Safety Coordinator to join our Stirling, Scotland team. You will contribute to the pharmacovigilance process, distributing safety reports, maintaining trackers, and coordinating with Clinical Operations, Data Management and Regulatory Submissions to support regulatory timelines.
Ideal candidates hold a science degree and have 1+ years in clinical trial safety, with strong attention to detail and proficiency in Microsoft Office.
#J-18808-LjbffrClinical Safety Coordinator — Flexible Growth & Impact 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.
