Associate Clinical Trial Manager – PhD/Post-Doc (CVRM)
Location: Navi Mumbai, India
Job Description:
Medpace is seeking a PhD or Post-Doctoral Life Sciences professional to join our Clinical Trial Management team as an Associate Clinical Trial Manager (aCTM). This full-time position is tailored for individuals with a strong academic background—particularly in Cardiovascular, Renal & Metabolic Disease (CVRM)—who are eager to transition into the clinical research industry. The aCTM will play a crucial support role in clinical trial execution, assisting Project Coordinators and CTMs in global study oversight and trial delivery.
Key Responsibilities:
Collaborate on global clinical study activities, working closely with Clinical Trial Managers and Project Coordinators.
Ensure timely and accurate completion of recurring project tasks.
Compile and maintain project status reports using the Clinical Trial Management System (CTMS).
Communicate with Sponsors, study sites, internal teams, and external vendors.
Oversee and maintain the internal regulatory filing system.
Support supply chain logistics for study materials and equipment.
Develop and track project timelines to ensure on-time trial milestones.
Organize and lead project meetings, including minute documentation and follow-ups.
Qualifications:
PhD in Life Sciences (with a focus or experience in Cardiovascular, Renal & Metabolic Disease highly preferred).
Strong interest in applying academic and analytical skills to clinical research project management.
Fluent in English, with excellent presentation and communication abilities.
Comfortable working in a fast-paced, international team environment.
Experience in the CRO or pharmaceutical industry is advantageous but not required.
Strong computer proficiency (Microsoft Office, Excel, databases) and organizational skills.
Why Join Medpace?
Structured training and development for accelerated career growth in CTM.
Clear career advancement paths within global clinical operations.
Competitive salary and benefits package.
Generous paid time off and a flexible work environment.
Access to employee wellness programs, appreciation events, and a collaborative culture.
About Medpace:
Medpace is a global full-service CRO providing Phase I–IV development services to biotech, pharmaceutical, and medical device companies. With over 5,000 employees across 40+ countries and headquartered in Cincinnati, Ohio, Medpace specializes in therapeutic areas including oncology, CVRM, CNS, endocrinology, and infectious diseases.
Awards & Recognition:
Listed by Forbes as one of America's Most Successful Midsize Companies (2021–2024)
Multiple-time winner of CRO Leadership Awards for excellence in quality, capabilities, and reliability
Estimated Salary: ₹9 – ₹12 LPA (based on academic credentials and industry entry-level benchmarks)
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