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Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (Cvrm))

2+ years
Not Disclosed
10 Sept. 16, 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

Clinical Trial Manager – Cardiovascular, Renal & Metabolic Disease (CVRM)

Location: Navi Mumbai, India
Functional Area: Clinical Trial Management
Job ID: 10935
Employment Type: Full-time


Job Summary:

Medpace is seeking a Clinical Trial Manager (CTM) to lead global clinical research studies. The position is fully office-based in Mumbai, India. The CTM will oversee multiservice global clinical trials, manage study timelines and deliverables, and coordinate cross-functional teams, ensuring successful execution of clinical trials in Cardiovascular, Renal & Metabolic Disease (CVRM).

This role also involves interactions with sponsors, participation in bid defense meetings, and supporting the business development team.


Key Responsibilities:

  • Serve as project lead for multiservice global clinical trials.

  • Manage study timelines and project deliverables.

  • Coordinate all services contracted for the study, including clinical monitoring, study start-up, regulatory, contracts, safety, and medical monitoring.

  • Lead cross-functional study teams.

  • Attend bid defense meetings and support business development initiatives.

  • Ensure compliance with regional and global regulations and study protocols.


Qualifications:

  • Bachelor’s degree in a health-related field (Master’s or PhD preferred).

  • Minimum of 2 years clinical trial management experience in the Asia Pacific region, preferably in a CRO environment.

  • Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) studies.

  • Excellent written and spoken English communication skills.

  • Flexible, accountable, and comfortable working in a global environment.


Medpace Overview:

Medpace is a full-service Clinical Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries. The company leverages local regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas.


Why Medpace:

  • Flexible work environment.

  • Competitive compensation and benefits package.

  • Paid time off and structured career growth opportunities.

  • Company-sponsored employee appreciation events.

  • Employee health and wellness initiatives.

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

  • Multiple CRO Leadership Awards from Life Science Leader magazine.