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About Company

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 a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, antiviral, and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 people across 40+ countries.

Position Name :

Drug Safety Specialist

Organization :



B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences


1 to 2 Years


25,000 - 35,000 /month



We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. 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 degree in Healthcare related field (Nursing, Pharmacy, Pharmacology, etc.);
  • Clinical experience or Clinical Research, case processing, and Post-marketing Pharmacovigilance experience is preferred;
  • Proficient in English is required;
  • Proficient knowledge of Microsoft® Office;
  • Broad knowledge of medical terminology; and
  • Strong organizational and communication skills.

Application Link