Roles & Responsibilities
• Support Project Managers in eClinical system design, setup, and study configuration
• Assist in creation and maintenance of study-specific documentation and quality records
• Track, monitor, and report study metrics, timelines, and progress
• Coordinate with clients to collect requirements and resolve system-related queries
• Perform assigned eClinical and data management support activities to ensure data accuracy and compliance
Qualification
• Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, or other health-related discipline
Experience
• 1-2 years of experience in a pharmaceutical company or CRO environment (preferred)
• Freshers with strong aptitude for clinical research may also be considered
Skills
• Strong attention to detail and accuracy
• Proficiency in Microsoft Excel and Word
• Working knowledge of medical terminology
• Good communication and coordination skills
• Ability to work effectively in a global, process-driven environment
About the Company
Medpace is a global, full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services. Known for scientific rigor and operational excellence, Medpace supports biotechnology, medical device, and pharmaceutical companies worldwide, offering strong career growth opportunities in clinical research and data management.