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Medpace is hiring for the position of Clinical Safety Coordinator / Drug Safety Specialist in Navi Mumbai, Maharashtra. This is a full-time, office-based opportunity for candidates looking to build a career in Clinical Safety, Pharmacovigilance, and Clinical Research.
The selected candidate will be responsible for handling and processing adverse events from multiple sources, including clinical trials and post-marketing surveillance.
Job Details
- Company: Medpace
- Position: Drug Safety Specialist / Clinical Safety Coordinator
- Job Type: Full-time
- Work Mode: Office-based
- Location: Navi Mumbai, Maharashtra
- Department: Clinical Safety
- Experience: Clinical experience, Clinical Research, Case Processing, or Post-Marketing Pharmacovigilance experience preferred
Key Responsibilities
The Clinical Safety Coordinator will support Medpace’s clinical safety operations and will be responsible for:
- Determining the appropriate plan of action for incoming calls.
- Collecting, processing, and tracking adverse events (AEs) and serious adverse events (SAEs).
- Preparing and writing safety narratives.
- Reporting and maintaining various safety data.
- Working closely with internal departments and investigative clinical research sites.
- Ensuring compliance with established clinical safety and pharmacovigilance processes.
- Supporting the accurate and timely handling of safety information from clinical trials and post-marketing sources.
Eligibility Criteria
Candidates applying for the Medpace Clinical Safety Coordinator position should meet the following requirements:
- Bachelor’s degree in a healthcare-related field such as Nursing, Pharmacy, Pharmacology, or a related discipline.
- Clinical experience or experience in Clinical Research, Case Processing, or Post-Marketing Pharmacovigilance is preferred.
- Strong English communication skills are required.
- Proficiency in Microsoft Office applications.
- Good knowledge of medical terminology.
- Strong organizational and communication skills.
- Ability to collaborate effectively with internal teams and clinical research sites.
About Medpace
Medpace is a global Contract Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
The company works across major therapeutic areas, including oncology, cardiology, metabolic and endocrinology, central nervous system, and anti-viral and anti-infective research.
Medpace is headquartered in Cincinnati, Ohio, and has a global workforce of more than 6,500 employees across 40+ countries.
Why Join Medpace?
This opportunity offers candidates the chance to work alongside physicians, scientists, and other clinical research professionals involved in the development of medical therapeutics.
Employees can benefit from:
- Purpose-driven work focused on advancing clinical research.
- Collaboration with experienced healthcare and clinical research professionals.
- Opportunities for continuous learning and professional development.
- An interactive and collaborative work environment.
- Exposure to global clinical safety and pharmacovigilance operations.
- A culture that encourages decision-making, creative thinking, and open communication.
Who Should Apply?
This position can be a good opportunity for Pharmacy, Pharmacology, Nursing, Clinical Research, and Pharmacovigilance professionals who want to develop their careers in clinical safety.
Candidates with relevant experience in adverse event processing, case processing, clinical research, or post-marketing pharmacovigilance are particularly encouraged to apply.
How to Apply
Interested and eligible candidates can apply through the Medpace job opening for the Clinical Safety Coordinator / Drug Safety Specialist position in Navi Mumbai.
Location: Navi Mumbai, Maharashtra, India
Note: Candidates should review the official job posting for the latest eligibility requirements and application details before applying.
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