Clinical Safety Specialist

2 weeks ago


Cincinnati, Ohio, United States Medpace Full time
Clinical Safety Coordinator Job Description

We are seeking a skilled Clinical Safety Coordinator to join our team at Medpace, a leading full-service clinical contract research organization (CRO). As a Clinical Safety Coordinator, you will play a critical role in ensuring the safety of patients participating in clinical trials and post-marketing surveillance.

Key Responsibilities:
  • 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
Requirements:
  • Bachelor's degree in life/health science, including Microbiology, Biology, Nursing, Pharmaceutical Science, Chemistry, or related field
  • Clinical experience or Clinical Research/Post marketing Pharmacovigilance experience is preferred
  • Proficient knowledge of Microsoft Office
  • Broad knowledge of medical terminology
  • Strong organizational and communication skills
About Medpace:

Medpace is a global CRO with over 30 years of experience in accelerating the development of safe and effective medical therapeutics. We leverage local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective.

As a Medpace employee, you will have the opportunity to work with a talented team of professionals who share your passion for improving patient outcomes. We offer a competitive compensation and benefits package, flexible work schedule, and opportunities for professional growth and development.



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