Medpace, Inc.
Location
Cincinnati, Ohio
The Clinical Safety Nurse will handle and process adverse events from various sources, including clinical trials and post-marketing surveillance. Responsibilities include determining action plans for incoming calls, collecting and tracking adverse events, writing safety narratives, and collaborating with internal departments.
Candidates must have a Bachelor's of Science in Nursing and preferably clinical experience or experience in clinical research/post-marketing pharmacovigilance. Proficiency in Microsoft Office and a broad knowledge of medical terminology are also required.
We are currently seeking a full-time, office-based Clinical Safety Nurse 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!
Determine plan of action for incoming calls; Collect, process, and track incoming adverse and serious adverse events; Write safety narratives; Report on various safety data; and Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Bachelor's of Science in Nursing; Clinical experience or Clinical Research/Post marketing Pharmacovigilance experience is preferred; Proficient knowledge of Microsoft® Office; Broad knowledge of medical terminology; and Strong organizational and communication skills.
Why Medpace?
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