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

2+ years
Not Disclosed
10 May 1, 2025
Job Description
Job Type: Full Time Education: PhD/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

Job Title: Clinical Trial Manager (Cardiovascular, Renal & Metabolic Disease - CVRM)
Company: Medpace
Location: Navi Mumbai, India
Department: Clinical Trial Management
Job ID: 10935

Job Summary:
Medpace is seeking an experienced Clinical Trial Manager (CTM) to lead global multiservice clinical trials within the Cardiovascular, Renal & Metabolic Disease (CVRM) domain. This full-time, office-based role in Navi Mumbai offers an opportunity to work with a scientifically driven organization that empowers its project teams to fully execute and manage clinical trials.

Key Responsibilities:

  • Serve as the project lead for global, multiservice clinical trials.

  • Manage sponsor communications, project deliverables, and timelines.

  • Coordinate across all contracted services, ensuring alignment with trial objectives.

  • Lead a cross-functional team comprising monitoring, study start-up, regulatory, contracts, medical monitoring, and safety.

  • Attend bid defense meetings and contribute to business development initiatives.

Qualifications:

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

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

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

  • Proficient in written and verbal English communication.

  • Demonstrated flexibility, accountability, and comfort working in a global setup.

About Medpace:
Medpace is a full-service CRO offering Phase I–IV clinical development support to biotech, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals in more than 40 countries. The organization applies a scientific, disciplined approach to accelerate the development of effective medical therapeutics.

Why Join Medpace?

  • Flexible work environment

  • Competitive salary and benefits

  • Attractive paid time off packages

  • Defined career advancement paths

  • Employee appreciation initiatives

  • Comprehensive wellness programs

Awards & Recognition:

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

  • Recipient of multiple CRO Leadership Awards from Life Science Leader magazine

What Happens Next:
Qualified candidates will be contacted by a Medpace representative regarding the next steps in the recruitment process.

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