Job Title: Associate Clinical Trial Manager (aCTM) – PhD / Post-Doc
Company: Medpace
Location: Navi Mumbai, India
Job Type: Full-time
Department: Clinical Trial Management
Job ID: 10936
Role Summary:
The Associate Clinical Trial Manager (aCTM) will support Clinical Trial Managers and Project Coordinators in planning, executing, and overseeing clinical trials, particularly in Cardiovascular, Renal, Metabolic, and Gastrointestinal therapeutic areas. This role is ideal for recent PhD graduates or Post-Doctoral researchers seeking to transition into clinical trial management within a CRO environment.
Key Responsibilities:
Communicate and collaborate on global study activities with internal teams, Sponsors, study sites, and third-party vendors.
Ensure timely delivery of recurring tasks with high accuracy.
Compile and maintain project-specific status reports in the clinical trial management system.
Provide oversight and quality control of internal regulatory filing systems.
Manage and oversee study supplies.
Create and maintain project timelines.
Coordinate project meetings and produce high-quality meeting minutes.
Qualifications:
PhD in Life Sciences.
Research experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal areas.
Fluency in English with strong presentation skills.
Ability to work in a fast-paced, dynamic, international environment.
Prior experience in a CRO or pharmaceutical industry is advantageous but not required.
Proficiency in computer applications (Word, Excel, databases, Windows).
Strong organizational and communication skills.
Skills & Competencies:
Analytical and academic skills applied to clinical project administration.
Attention to detail and high level of accuracy.
Ability to manage multiple priorities and timelines.
Collaborative and effective communication with cross-functional teams.
Company Overview:
Medpace is a full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. The company leverages regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries.
Why Join Medpace:
Flexible work environment.
Competitive compensation and benefits.
Generous PTO and structured career paths.
Employee appreciation events and wellness initiatives.
Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).
CRO Leadership Awards from Life Science Leader magazine.
Next Steps:
Applications will be reviewed by the Medpace team; qualified candidates will be contacted for further steps in the hiring process.
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