Clinical Project Coordinator – Entry Level | Medpace Careers in Navi Mumbai for clinical research jobs
Looking to launch your career in clinical research? Medpace is hiring a Clinical Project Coordinator (Entry Level) in Navi Mumbai! Join a global leader in clinical trial management and step into one of the most promising clinical research jobs in India. If you’re a life science graduate ready to make a meaningful impact, this role is the perfect start to your Medpace career journey.
About the Company:
Medpace is a full-service Clinical Research Organization (CRO) dedicated to advancing medical breakthroughs through science-driven innovation. Headquartered in Cincinnati, Ohio, Medpace operates in over 40 countries and employs 5,000+ professionals. The company provides Phase I–IV clinical trial management services to the biotechnology, pharmaceutical, and medical device industries. Recognized by Forbes and Life Science Leader magazine, Medpace careers promise growth, purpose, and a passion for improving global health.
Job Details:
- Assist in daily coordination of clinical research projects.
- Collaborate with Clinical Trial Managers for project timelines and deliverables.
- Prepare and maintain study-specific documentation and reports.
- Manage CTMS updates, eTMF QC, and enrollment tracking.
- Coordinate site feasibility, activation, and study supply logistics.
- Communicate effectively with cross-functional teams, vendors, and sponsors.
- Contribute to maintaining compliance and quality standards in clinical trial management.
Educational Requirements:
- Bachelor’s degree in a Life Sciences field (Biotechnology, Microbiology, Pharmacology, or related disciplines).
- Strong understanding of clinical research fundamentals and documentation practices.
- Excellent communication, coordination, and computer skills (Word, Excel, CTMS familiarity preferred).
Key Responsibilities:
- Support day-to-day clinical trial management activities.
- Update project trackers, status reports, and eTMF records.
- Assist the CTM with site feasibility, activation, and document preparation.
- Communicate with regional teams, vendors, and sponsors.
- Maintain study-specific guidelines and ensure quality compliance.
Skills Required:
- Excellent organizational and multitasking skills.
- Proficiency in Microsoft Office and clinical documentation tools.
- Detail-oriented with a proactive mindset.
- Strong interpersonal and communication skills.
- Ability to work collaboratively in cross-functional clinical research teams.
Step into the world of clinical research jobs with a globally recognized leader! Medpace offers a nurturing environment, structured career paths, and the opportunity to contribute to global medical innovation. If you’re passionate about science, collaboration, and growth, Medpace careers will help you build a strong foundation in clinical trial management.
