Medpace, Inc.
Location
Cincinnati, Ohio
The Clinical Safety Coordinator will collect, process, and track serious adverse event reports while generating safety narratives and performing quality control of safety cases. Collaboration with internal departments and clinical research sites is essential to ensure compliance with safety processes.
Candidates must have a Bachelor’s degree in a life or health science field and possess proficient knowledge of Microsoft Office. A broad understanding of medical terminology and strong organizational and communication skills are also required.
We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance. 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!
Collect, process, and track serious adverse event (SAE) reports Generate safety narratives and queries Safety database data entry Perform quality control of safety cases Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Bachelor’s degree in life/health science including, but not limited to, Microbiology, Biology, Pharmaceutical Science, Chemistry, or related field; Proficient knowledge of Microsoft® Office; Broad knowledge of medical terminology; and Strong organizational and communication skills.
Why Medpace?
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