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.

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 chance for you!

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.

Qualifications
Bachelors 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
Solid organizational and communication skills.

Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Drug Safety Specialist/ Clinical Safety Coordinator Navi Mumbai
🏢 Medpace Clinical Research India
📍 Navi Mumbai