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

0-2 years
Not Disclosed
10 March 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 Disease (CVRM)) (Navi Mumbai, India)

Employer: Medpace
Industry: Clinical Research (CRO)
Department: Clinical Trial Management
Employment Type: Full-Time
Location: Navi Mumbai, India

Job Summary:

Medpace is hiring an Associate Clinical Trial Manager (aCTM) for PhD/Post-Doctoral candidates to join its Clinical Trial Management team in Mumbai. This role supports Project Coordinators and Clinical Trial Managers in project management activities. It is an excellent opportunity for recent PhD graduates to transition into clinical research, gain industry experience, and receive intensive training for an accelerated Clinical Trial Management career path.

Responsibilities:

  • Collaborate on global study activities with project teams.
  • Ensure timely and accurate delivery of recurrent project tasks.
  • Maintain project-specific reports within the clinical trial management system.
  • Interact with internal teams, sponsors, study sites, and vendors.
  • Oversee regulatory filing systems and study supplies management.
  • Create and maintain project timelines.
  • Coordinate project meetings and document high-quality meeting minutes.

Qualifications:

  • PhD in Life Sciences (specialization in Cardiovascular, Renal & Metabolic Disease (CVRM) preferred).
  • Fluency in English with strong presentation skills.
  • Ability to work in a fast-paced, global environment.
  • Experience in the CRO or pharmaceutical industry is advantageous but not required.
  • Proficiency in Microsoft Office (Word, Excel, databases).

Why Join Medpace?

  • Competitive salary, benefits, and PTO packages.
  • Clear career growth opportunities with structured training.
  • Flexible work environment with employee appreciation programs.
  • Recognized as one of America's Most Successful Midsize Companies (Forbes, 2021-2024).

About Medpace:

Medpace is a global clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace operates in 40+ countries with 5,000+ employees worldwide.