eClinical Coordinator
Company: Medpace
Location: Navi Mumbai, India
Department: Data Management / eClinical
Job Type: Full-Time
Experience Required: 1–2 Years (Preferred)
Education: Bachelor’s Degree in a Health-Related Field
About Medpace
Medpace is a global full-service Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies. With headquarters in Cincinnati, Ohio, and operations in more than 40 countries, Medpace supports clinical research across major therapeutic areas including oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, and infectious diseases. The company’s mission is to accelerate the development of safe and effective medical therapies through scientific expertise and disciplined clinical research processes.
Job Overview
Medpace is seeking a detail-oriented eClinical Coordinator to join its Data Management / eClinical team in Navi Mumbai, India. In this role, you will work closely with the eClinical Project Manager and cross-functional teams to ensure the accuracy and integrity of patient-reported clinical study data. The position offers a structured work environment with comprehensive onboarding and training programs designed to help employees build expertise in eClinical systems and clinical data management processes.
Key Responsibilities
Assist the eClinical Project Manager with clinical system design, configuration, and study setup
Develop and maintain study-specific documentation related to eClinical systems
Track project progress and generate key study metrics and monitoring reports
Support project teams in maintaining accurate clinical study data and ensuring data quality standards
Collaborate with clients to gather system requirements and respond to project-related inquiries
Assist in the implementation and management of electronic clinical data collection systems
Contribute to project coordination activities and complete additional assigned tasks to support clinical study operations
Required Skills and Qualifications
Bachelor’s degree in a health-related discipline such as Life Sciences, Pharmacy, Nursing, or Biotechnology
Strong attention to detail and organizational skills
Working knowledge of Microsoft Excel and Microsoft Word
Basic understanding of medical terminology
Prior experience (1–2 years preferred) in a pharmaceutical company or Contract Research Organization (CRO) environment
Ability to work collaboratively with cross-functional teams in clinical research projects
Travel Requirements
No travel required for this role
Why Join Medpace
Medpace offers a dynamic work environment that supports professional development and career growth within the clinical research industry. Employees benefit from structured training programs, exposure to global clinical trials, and opportunities to build expertise in clinical data management and eClinical technologies.
Employee Benefits
Flexible work environment
Competitive compensation and benefits package
Competitive paid time off (PTO) programs
Structured career development and growth opportunities
Employee recognition and appreciation programs
Health and wellness initiatives
Awards and Recognition
Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023, and 2024
Recipient of multiple CRO Leadership Awards from Life Science Leader magazine for expertise, quality, reliability, and capabilities in clinical research services
Application Process
Applications will be reviewed by the Medpace recruitment team. Candidates whose qualifications match the role requirements will be contacted with details regarding the next steps in the selection process.
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