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

2+ years
Not Disclosed
10 May 1, 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

Job Title: Associate Clinical Trial Manager – PhD / Post-Doc (Cardiovascular, Renal & Metabolic Disease - CVRM)
Company: Medpace
Location: Navi Mumbai, India
Department: Clinical Trial Management
Job ID: 10936

Job Summary:
Medpace, a leading global CRO, is hiring full-time Associate Clinical Trial Managers (aCTM) with PhD or Post-Doctoral experience to join its Clinical Trial Management team in Navi Mumbai. This role is ideal for recent PhD graduates or post-doc researchers aiming to enter the clinical research industry and accelerate their growth into Clinical Trial Management. The selected candidate will support Project Coordinators and Clinical Trial Managers in various project management functions related to cutting-edge therapeutics in Cardiovascular, Renal & Metabolic Diseases (CVRM).

Key Responsibilities:

  • Collaborate globally with study teams, project coordinators, and CTMs.

  • Ensure timely and accurate completion of recurring clinical trial tasks.

  • Maintain project-specific reports and documentation within the clinical trial management system.

  • Interact with internal teams, sponsors, study sites, and third-party vendors.

  • Oversee internal regulatory filing systems and manage related quality control processes.

  • Supervise study supplies and maintain oversight.

  • Develop and maintain project timelines.

  • Schedule project meetings and generate detailed meeting minutes.

Qualifications:

  • PhD in Life Sciences.

  • Research experience or familiarity with Cardiovascular, Renal & Metabolic Disease (CVRM).

  • Strong English communication and presentation skills.

  • Ability to excel in a fast-paced, international clinical environment.

  • Prior industry experience in a CRO or pharmaceutical setting is beneficial but not mandatory.

  • Proficient in Microsoft Office tools and database systems.

  • Excellent organizational and interpersonal skills.

About Medpace:
Medpace is a full-service clinical contract research organization (CRO) supporting Phase I–IV clinical trials for the biotech, pharmaceutical, and medical device sectors. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries, providing scientific and regulatory expertise across major therapeutic areas, including CVRM, oncology, neurology, and infectious diseases.

Why Join Medpace?

  • Flexible work environment

  • Competitive compensation and benefits

  • Generous paid time off

  • Structured growth opportunities

  • Health and wellness programs

  • Company-sponsored appreciation events

Awards & Recognition:

  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)

  • Consistently awarded CRO Leadership honors by Life Science Leader magazine

What Happens Next:
Qualified applicants will be contacted by a Medpace recruiter for next steps in the selection process.

EO/AA Employer: M/F/Disability/Vets