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Clinical Research Jobs in Mumbai – Medpace Careers | Life Science Graduates Apply
Looking for exciting Clinical Research Jobs in Mumbai? Medpace, a global leader in clinical development, is hiring a Clinical Project Coordinator – Entry Level in Navi Mumbai, India. This full-time opportunity is ideal for life science graduates eager to begin a career in clinical trial management. As part of Medpace Careers, you’ll gain hands-on experience in global research projects and contribute to innovations that advance public health.
Job Details:
- Job Position: Clinical Project Coordinator – Entry Level
- Location: Navi Mumbai, India
- Department: Clinical Trial Management
- Job ID: 11719
About the Company
Medpace is a global, full-service clinical research organization (CRO) dedicated to accelerating the development of safe and effective medical therapeutics. As part of Medpace Careers, employees contribute to groundbreaking clinical studies that improve patient outcomes worldwide. The company is renowned for its scientific expertise, collaborative culture, and opportunities for professional growth.
Qualifications:
- Bachelor’s degree in a Life Sciences discipline.
- Strong organizational and communication skills.
- Proficiency in Microsoft Office (Word, Excel, and databases).
- Ability to present and coordinate effectively in internal and external meetings.
Job Description:
Medpace is currently seeking a full-time, office-based Clinical Project Coordinator – Entry Level to join its Clinical Trial Management team in India. This role is ideal for those seeking Clinical Research Jobs in Mumbai, offering a chance to work with cross-functional teams on global projects. As part of Medpace Careers, you will play a key role in supporting the planning and execution of clinical trials that shape the future of medicine.
Clinical Research Job – Key Responsibilities:
- Manage day-to-day clinical trial operations.
- Collaborate closely with the Clinical Trial Manager (CTM) to ensure accurate and timely task delivery.
- Compile and maintain project-specific status reports.
- Update the Clinical Trial Management System (CTMS) with study milestones and enrollment data.
- Perform ongoing eTMF (electronic Trial Master File) updates and quality checks.
- Assist in drafting study plans and study-specific documentation.
- Support site feasibility assessments, site activation, and study supply management.
- Communicate effectively with sponsors, vendors, and internal teams.
