Associate Clinical Trial Manager – CRO Jobs | Medpace Careers | Life Sciences Jobs | Apply Now
Are you actively exploring CRO Jobs that allow you to move from research to real-world clinical development? Medpace Careers presents an exciting pathway for PhD and postdoctoral professionals seeking advanced Life Sciences Jobs in clinical trial management. This role offers structured training, international exposure, and an accelerated career path into Clinical Trial Management for candidates ready to grow beyond academia.
- Job Title: Associate Clinical Trial Manager – PhD / Post-Doc
- Location: Navi Mumbai, India
- Department: Clinical Trial Management
- Job ID: 11837
About the Company:
Medpace is a full-service clinical contract research organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies worldwide. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries and is known for its scientific, disciplined, and global approach to clinical research.
Job Overview:
The Associate Clinical Trial Manager (aCTM) role is a full-time, on-site position based in Navi Mumbai. The role supports global clinical studies across therapeutic areas such as cardiovascular, renal, metabolic, and gastrointestinal research. The Associate Clinical Trial Manager collaborates with internal teams, sponsors, study sites, and vendors while supporting timelines, documentation, regulatory systems, and overall project coordination.
Educational Requirements:
- PhD in Life Sciences
- Post-Doctoral research experience in cardiovascular, renal, metabolic, or gastrointestinal areas
Key Responsibilities:
- Communicate and collaborate on global clinical study activities
- Support Project Coordinators and Clinical Trial Managers
- Ensure timely completion of recurring project tasks
- Compile and maintain project status reports
- Interact with sponsors, study sites, and third-party vendors
- Provide oversight of regulatory filing systems
- Manage study supplies and documentation
- Create and maintain project timelines
- Coordinate meetings and prepare accurate meeting minutes
Skills Required:
- Strong analytical and research background
- Excellent written and verbal English communication skills
- Ability to work in fast-paced, international CRO environments
- Proficiency in Excel, databases, and clinical documentation tools
- Strong organizational and project coordination skills
- Interest in clinical trial management and industry research
These CRO Jobs at Medpace offer a powerful entry point for PhD and Post-Doctoral researchers seeking long-term careers in clinical development. With structured training, global exposure, and rapid growth opportunities, this role is ideal for candidates aiming to transition into impactful Life Sciences Jobs within the clinical research industry.
