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

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

Clinical Trial Manager – 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 seeking an experienced Clinical Trial Manager (CTM) to lead global clinical research studies. This is a fully office-based position in Mumbai, India. As a scientifically led organization, Medpace provides full-service clinical trial execution, empowering project teams to lead and manage studies efficiently.

Responsibilities:

  • Serve as the project lead for multiservice global clinical trials.
  • Manage sponsor interactions, project timelines, and deliverables.
  • Coordinate contracted services for the study.
  • Lead cross-functional teams, including clinical monitoring, regulatory, contracts, safety, and medical monitoring.
  • Participate in bid defense meetings and support the business development team in securing new projects.

Qualifications:

  • Bachelor’s degree in a health-related field (Master’s or PhD preferred).
  • At least two years of clinical trial management experience in the Asia-Pacific region (preferably in a CRO).
  • Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) studies is required.
  • Strong communication skills in written and spoken English.
  • Ability to work in a flexible, accountable, and global environment.

Why Join Medpace?

  • Competitive salary, benefits, and PTO packages.
  • 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 full-service clinical contract research organization (CRO) providing 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.