Explore rewarding CRO jobs at Medpace in Navi Mumbai. Openings for Medical Writer, Drug Safety Specialist, and Safety Database roles in clinical research and pharmacovigilance careers in India.
About the Company
Medpace is a globally recognized full-service Clinical Contract Research Organization (CRO) providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across more than 40 countries.
With a scientific and disciplined approach, the company accelerates the development of safe and effective therapeutics in key areas including oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective.
Medpace is consistently awarded for expertise, quality, and reliability, including Forbes recognition as one of America’s Most Successful Midsize Companies (2021–2024) and CRO Leadership Awards.
Job Details
- Company Name: Medpace
- Location: Navi Mumbai, India
- Work Type: Full-time, Office-based
Job Description
Medpace is expanding its India operations and seeking talented professionals for office-based roles in Navi Mumbai. These positions support global clinical trials and pharmacovigilance activities within Core Labs and Clinical Safety departments, offering opportunities to contribute to life-changing medical advancements.
Medical Writer (Core Labs)
- Job ID: 11938
- Department: Core Labs
- Role: Generate, revise, and maintain clinical documents with quality control and input on data analysis
- Experience: Not explicitly required; suitable for candidates with relevant scientific background
- Education/Qualification: Master’s degree in a health or science-related field
Drug Safety Specialist / Clinical Safety Coordinator (Nursing Professionals Encouraged)
- Job ID: 11946
- Department: Clinical Safety
- Role: Process adverse events, write safety narratives, and ensure regulatory compliance
- Experience: Clinical research, case processing, or post-marketing pharmacovigilance experience preferred
- Education/Qualification: Bachelor’s degree in Healthcare-related field (Nursing, Pharmacy, Pharmacology, etc.)
Safety Database Specialist
- Job ID: 11954
- Department: Clinical Safety
- Role: Manage safety database configuration, reporting, UAT, and support periodic safety reports
- Experience: 1-2 years of directly related experience
- Education/Qualification: Bachelor’s degree in scientific discipline, Business Informatics, or similar
Skills/Qualifications
- Advanced degree (Master’s or Bachelor’s) in health, science, or related field
- Strong oral and written communication skills in English
- Intermediate to broad knowledge of medical terminology and clinical patient management
- Proficiency in Microsoft Office
- Organizational skills and attention to detail
- Experience with safety databases (Argus/Argus J preferred for Database role)
- SQL, OBIEE reporting, or pharmacovigilance knowledge advantageous
Key Responsibilities
Medical Writer (Core Labs):
- Generate, revise, and maintain clinical documents
- Coordinate quality control and maintain audit trails
- Provide input on data analysis planning and document outcomes
- Perform additional assigned duties
Drug Safety Specialist / Clinical Safety Coordinator:
- Collect, process, and track adverse/serious adverse events
- Write safety narratives
- Determine action plans for incoming safety calls
- Report safety data and collaborate on compliance
- Work with sites and internal teams
Safety Database Specialist:
- Configure systems (product, study, license) in Argus/Argus J
- Create reports using Oracle Business Intelligence
- Resolve database issues and execute UAT
- Generate outputs for DSUR, PSUR, PBRER
- Support inspections, audits, and SOP development
Benefits/Perks
- Flexible work environment
- Competitive compensation and benefits package
- Generous PTO packages
- Structured career paths with professional growth opportunities
- Company-sponsored employee appreciation events
- Health and wellness initiatives
- Opportunity to impact global patient outcomes
How to Apply
Apply online through the official Medpace careers portal at https://careers.medpace.com/. Search by location (Navi Mumbai, India) or requisition numbers: 11938 (Medical Writer), 11946 (Drug Safety), 11954 (Safety Database Specialist).
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Medpace Career page.
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Take the next step in your CRO career—apply now and join a team making a real difference!
Why You Should Join
At Medpace, you’ll contribute to meaningful work that positively impacts patients worldwide across diverse therapeutic areas. With over 30 years of excellence, the company offers purpose-driven roles, passionate collaboration, and long-term stability in a growing global CRO.
Enjoy professional development, recognition, and an environment focused on scientific innovation and employee well-being.
FAQs
What qualifications are needed for these Medpace roles?
Qualifications vary: Master’s in health/science for Medical Writer; Bachelor’s in healthcare (nursing/pharmacy preferred) for Drug Safety; Bachelor’s in science/informatics with 1-2 years experience for Database Specialist.
How do I apply for jobs at Medpace India?
Are these positions remote or office-based?
All roles are full-time and office-based in Navi Mumbai, India.
What career growth can I expect at Medpace?
Medpace offers structured career paths, professional training, global exposure, and opportunities to advance in clinical research and pharmacovigilance within a leading CRO.