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
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 of Science in Nursing (BSN) or higher (MSc Nursing preferred)
Clinical experience in a hospital or healthcare setting
Proficient knowledge of Microsoft® Office;
Broad knowledge of medical terminology; and
Strong organizational and communication skills.
Medpace Overview
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 secure 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.
Why Medpace?
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