The pharmaceutical and clinical research industry is constantly evolving, and with it, the demand for highly skilled professionals in pharmacovigilance and drug safety continues to rise. Medpace, a global and leading full-service clinical contract research organization (CRO), is currently seeking dedicated and passionate professionals for the position of Drug Safety Specialist/Clinical Safety Coordinator in Navi Mumbai, Maharashtra, India.

Drug Safety Specialist/ Clinical Safety Coordinator

Navi Mumbai, Maharashtra, India

About the Job

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!

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

• 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.

How to Apply?

If you have a passion for drug safety and want to contribute to global healthcare advancements, this opportunity is perfect for you! Interested candidates can apply directly through Medpace’s career portal