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Clinical Safety Specialist

2 months ago

Cincinnati, Ohio, United States Medpace Full time
Job Summary:

We are seeking a full-time Clinical Safety Nurse to join our Clinical Safety department. This position will be focused on handling and processing adverse events from all sources, including clinical trials and post-marketing surveillance.

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
Qualifications:
  • Bachelor's degree in life/health science, including but not limited to, 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 full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.

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.

Why Medpace?

At Medpace, we are committed to making a difference in the lives of patients and families affected by disease. We strive to create a work environment that is collaborative, inclusive, and supportive of our employees' growth and development.

We offer a competitive compensation and benefits package, flexible work schedule, and opportunities for professional growth and development.