Pharma Jobs in Mumbai: Medpace is Hiring a Drug Safety Specialist
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If you are searching for Pharma Jobs in Mumbai, kickstart your global career in clinical research with Medpace as a Drug Safety Specialist / Clinical Safety Coordinator in Navi Mumbai. This role offers an opportunity to contribute to global drug safety by managing and processing adverse event data from clinical trials and post-marketing surveillance. Join Medpace’s expert team and be part of a mission-driven organization committed to advancing safe and effective medical therapies worldwide.
Job Details:
- Job Title: Drug Safety Specialist / Clinical Safety Coordinator
- Location: Navi Mumbai, India
- Department: Clinical Safety
- Job ID: 10603
Job Summary:
Medpace is currently seeking a full-time, office-based Clinical Safety Coordinator to join the Clinical Safety department in India. This position focuses on handling and processing adverse events from all sources, including clinical trials and post-marketing surveillance.
If you’re looking for an exciting career that allows you to apply your expertise and grow within the field of pharmacovigilance, this is the perfect opportunity.
About the Company:
Medpace is a leading global Clinical Research Organization (CRO) headquartered in Cincinnati, Ohio, USA, with operations in over 40 countries worldwide. For more than 30 years, Medpace has been at the forefront of clinical research, partnering with pharmaceutical, biotechnology, and medical device companies to accelerate the development of safe and effective medical therapies. The company offers comprehensive Phase I–IV clinical development services, combining scientific expertise, advanced technology, and a disciplined approach to ensure efficiency, quality, and regulatory compliance across all stages of the drug development process. Medpace’s therapeutic expertise spans a wide range of areas, including oncology, cardiology, endocrinology, metabolic disorders, infectious diseases, and central nervous system (CNS) research. Driven by its core values — People, Purpose, and Passion — Medpace fosters a collaborative environment that empowers employees to make a meaningful impact on global health. With a commitment to excellence and innovation, Medpace continues to play a crucial role in bringing breakthrough treatments to patients worldwide.
Education:
Bachelor’s degree in a healthcare-related field (Nursing, Pharmacy, Pharmacology, etc.).
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 clinical research sites to ensure compliance with safety processes.
Skills:
- Experience in Clinical Research, Case Processing, or Post-Marketing Pharmacovigilance preferred.
- Proficient English communication skills.
- Strong working knowledge of Microsoft Office.
- Broad understanding of medical terminology.
- Excellent organizational and communication skills.
