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.

Why Join Medpace?

Medpace offers a dynamic and growth-oriented environment for professionals looking to make a mark in the pharmaceutical and clinical research industry. As a Drug Safety Specialist/ Clinical Safety Coordinator, you will play a vital role in ensuring patient safety and regulatory compliance while gaining hands-on experience in pharmacovigilance and clinical trials.

How to Apply?

If you are passionate about clinical safety and looking for a rewarding career opportunity, apply today! Visit Medpace’s official website OR