A complete application in a minute
Tailored resume and cover letter, ready to send.
Medpace in India is seeking a full-time, office-based Clinical Safety Coordinator Entry to join our Clinical Safety department. This role focuses on handling and processing adverse events from clinical trials and post-marketing surveillance.
You will collect, process, and track adverse events, write safety narratives, report safety data, and collaborate with internal teams to ensure compliance with safety processes.
We are currently seeking a full-time, office-based Clinical Safety Coordinator Entry 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!
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Please note benefits may vary based on country.