Associate Clinical Trial Manager (PhD / Post-Doc) – CVRM
Location: Navi Mumbai, India
Functional Area: Clinical Trial Management
Job ID: 10936
Employment Type: Full-time
Job Summary:
Medpace, a leading CRO for Biotech companies, is seeking PhD and/or Post-Doctoral Research candidates for the role of Associate Clinical Trial Manager (aCTM) in Navi Mumbai, India. The aCTM will support Project Coordinators and Clinical Trial Managers in performing project management activities for clinical trials in Cardiovascular, Renal & Metabolic Disease (CVRM).
This role is ideal for recent PhD graduates seeking to transition into the clinical research industry, gain foundational training, and accelerate their career in Clinical Trial Management (CTM).
Key Responsibilities:
Communicate and collaborate on global study activities, working closely with Project Coordinators and Clinical Trial Managers.
Ensure timely and accurate delivery of recurrent project tasks.
Compile and maintain project-specific status reports within the clinical trial management system.
Interact with internal project teams, sponsors, study sites, and third-party vendors.
Provide oversight and quality control of internal regulatory filing systems.
Manage and monitor study supplies.
Create and maintain project timelines.
Coordinate project meetings and produce high-quality minutes.
Qualifications:
PhD in Life Sciences.
Experience or knowledge in Cardiovascular, Renal & Metabolic Disease (CVRM).
Fluent in English with strong presentation skills.
Ability to work in a fast-paced, dynamic international environment.
Prior experience in CRO or pharmaceutical industry is advantageous but not required.
Proficient in Microsoft Office, databases, Excel, and Windows.
Strong organizational and communication skills.
Medpace Overview:
Medpace is a full-service Clinical Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries. The company leverages local regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective therapeutic areas.
Why Medpace:
Flexible work environment.
Competitive compensation and benefits package.
Paid time off and structured career development opportunities.
Company-sponsored employee appreciation events.
Employee health and wellness initiatives.
Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).
Multiple CRO Leadership Awards from Life Science Leader magazine.
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