Instagram
youtube
Facebook

Associate Clinical Trial Manager - Phd / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (Cvrm))

3+ years
₹9 – ₹12 LPA
10 July 29, 2025
Job Description
Job Type: Full Time Education: PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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)