Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate Clinical Trial Manager - Phd / Post-Doc (Cardiovascular/Renal/Metabolic/Gastrointestinal)

0-2 years
Not Disclosed
10 Oct. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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 (Cardiovascular, Renal, Metabolic, Gastrointestinal)

📍 Location: Navi Mumbai, India
🏢 Department: Clinical Trial Management
🆔 Job ID: 10936


Job Summary

Medpace, a leading Clinical Research Organization (CRO) specializing in biotechnology, is seeking highly motivated candidates with PhD or Post-Doctoral research experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal areas.

This full-time Associate Clinical Trial Manager (aCTM) position is based in Navi Mumbai, India and offers a unique opportunity for recent PhD graduates to transition into the clinical research industry. You will support Clinical Trial Managers (CTMs) and Project Coordinators in managing and executing clinical projects across global teams.

The role includes comprehensive training, hands-on project experience, and an accelerated career path toward Clinical Trial Management.


Key Responsibilities

  • Collaborate with global teams on clinical study activities.

  • Support CTMs and Project Coordinators in daily project management tasks.

  • Ensure accurate and timely completion of recurring study deliverables.

  • Maintain project-specific reports and documentation in CTMS.

  • Communicate effectively with sponsors, study sites, vendors, and internal teams.

  • Provide oversight and quality control of regulatory filing systems.

  • Manage and track study supplies and project timelines.

  • Organize and document project meetings with detailed minutes.


Qualifications

  • Education: PhD in Life Sciences.

  • Experience: Research background in Cardiovascular, Renal, Metabolic, or Gastrointestinal fields.

  • Skills & Competencies:

    • Excellent communication and presentation skills (fluency in English required).

    • Strong organizational and computer proficiency (Word, Excel, databases, Windows).

    • Ability to thrive in a fast-paced, dynamic, and international environment.

    • Prior CRO or pharmaceutical experience preferred but not mandatory.


About Medpace

Medpace is a full-service CRO providing Phase I–IV clinical development services to biotech, pharmaceutical, and medical device industries.
Headquartered in Cincinnati, Ohio, Medpace employs 5,000+ professionals across 40+ countries and supports therapeutic areas such as Oncology, Cardiology, Metabolic Diseases, Endocrinology, CNS, Anti-viral, and Anti-infective research.

Mission:
Accelerate the global development of safe and effective medical therapeutics through scientific excellence and disciplined execution.


Why Join Medpace?

People. Purpose. Passion. Make a Difference Tomorrow — Join Us Today.

  • Flexible work environment

  • Competitive compensation and benefits

  • Generous PTO package

  • Structured career growth pathways

  • Company-sponsored employee appreciation events

  • Health and wellness programs


Awards & Recognition

🏅 Forbes: One of America’s Most Successful Midsize Companies (2021–2024)
🏅 Life Science Leader Magazine: Recipient of CRO Leadership Awards for expertise, reliability, quality, and compatibility


Next Steps

A Medpace team member will review your qualifications.
If shortlisted, you will be contacted for further steps.

Apply Now
🔗 Share via Social Media