Are you passionate about ensuring drug safety and making a meaningful impact in the pharmaceutical and clinical research industry? Medpace, a leading global clinical contract research organization (CRO), is seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in Navi Mumbai, India. This role focuses on handling and processing adverse events from clinical trials and post-marketing surveillance, ensuring compliance with global safety standards.
If you are looking for an exciting career where you can leverage your expertise in pharmacovigilance, clinical research, or healthcare, and grow professionally, this is the perfect opportunity for you!
Key Responsibilities
As a Clinical Safety Coordinator, you will:
- Determine the plan of action for incoming safety-related calls.
- Collect, process, and track adverse events (AEs) and serious adverse events (SAEs) from clinical trials and post-marketing sources.
- Write detailed safety narratives for regulatory submissions.
- Analyze and report on various safety data to ensure compliance with global regulations.
- Collaborate with internal departments and clinical research sites to maintain adherence to safety protocols.
Qualifications
To excel in this role, you should have:
- A Bachelor’s degree in a healthcare-related field such as Nursing, Pharmacy, Pharmacology, or a related discipline.
- Preferred experience in clinical research, case processing, or post-marketing pharmacovigilance.
- Proficiency in English (written and verbal) to ensure clear communication with global teams.
- Strong knowledge of medical terminology and Microsoft Office tools (Word, Excel, PowerPoint).
- Excellent organizational and communication skills to manage multiple tasks efficiently.
About Medpace
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. With over 30 years of experience, Medpace has been at the forefront of accelerating the development of safe and effective medical therapeutics.
Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 professionals across 40+ countries. Our therapeutic expertise spans oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, anti-viral, and anti-infective therapies.
Why Join Medpace?
At Medpace, we believe in People. Purpose. Passion. Our work directly impacts the lives of patients and families worldwide, and we are committed to making a difference in global healthcare.
Here’s why you should consider joining our team:
- Flexible work environment that promotes work-life balance.
- Competitive compensation and benefits package, including PTO.
- Structured career paths with opportunities for professional growth.
- Company-sponsored events and wellness initiatives to appreciate and support employees.
- Awards and Recognition:
- Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021, 2022, 2023, 2024).
- Consistently awarded CRO Leadership Awards by Life Science Leader magazine for expertise, quality, and reliability.
