Apply Online for Drug Safety Specialist at Medpace

Medpace, a global Clinical Research Organization (CRO) with headquarters in Cincinnati. USA. and an office in Lyon. France, is seeking CRA candidates to join our team. This position offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of patients.

Post : Drug Safety Specialist / Clinical Safety Coordinator

Job Summary
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.

Responsibilities
• 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.

Candidate Profile
• 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 English is required
• Proficient knowledge of Microsoft® Office;
• Broad knowledge of medical terminology; and
• Strong organizational and communication skills.

Additional Information
Qualification : Bachelor's degree in Nursing, Pharmacy, Pharmacology, etc
Location : Navi Mumbai, India
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Clinical Safety
End Date : 31st August 2026