Drug Safety Specialist/ Clinical Safety Coordinator at Medpace | Apply Online
A rare chance has emerged for aspiring Clinical Safety Coordinators at Medpace in Navi Mumbai, India. This full-time, office-based role is a Medpace careers opportunity focused on the handling and processing of adverse events from various sources, including clinical trials and post-marketing surveillance.
About the company
Medpace is a full-service clinical contract research organization (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. The organization’s mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. Medpace leverages 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, Medpace employs more than 6,500 people across 40+ countries.
Medpace Careers: Job Details
- Location: Navi Mumbai, India
- Department: Clinical Safety
- Reference Number: 11946
Job Description
The Clinical Safety Coordinator will be responsible for determining the plan of action for incoming calls, collecting, processing, and tracking incoming adverse and serious adverse events, writing safety narratives, reporting on various safety data, and collaborating with internal departments and investigative clinical research sites to ensure compliance with safety processes. This Medpace careers position supports essential safety-process coordination.
Key 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.
- Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Eligibility Criteria
- Bachelor’s degree in a 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.
- Strong organizational and communication skills.
Why Medpace?
When joining Medpace, individuals 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.
How to Apply
Conclusion
This Medpace careers opportunity for a Clinical Safety Coordinator is a significant step for qualified candidates looking to advance their careers in clinical safety. Interested individuals are encouraged to apply at the earliest.
