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

Medpace
Medpace
2+ years
₹15 – ₹22 LPA
10 July 29, 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)
Location: Navi Mumbai, India

Job Description:
Medpace is looking for an experienced Clinical Trial Manager (CTM) to lead global clinical research projects within the Cardiovascular, Renal & Metabolic Disease (CVRM) domain. This office-based position in Navi Mumbai offers an opportunity to manage end-to-end clinical trial execution and act as a key point of contact for sponsors, vendors, and internal stakeholders. If you're passionate about driving trial outcomes in a scientific, cross-functional environment, this role is ideal for you.

Key Responsibilities:

  • Serve as project lead on multi-service global clinical trials.

  • Ensure timely and successful delivery of project timelines and trial milestones.

  • Lead cross-functional teams including clinical monitoring, regulatory affairs, site start-up, contracts, safety, and medical monitoring.

  • Coordinate all contracted services to ensure protocol and regulatory compliance.

  • Collaborate and communicate directly with sponsors, providing trial updates, reports, and oversight.

  • Support business development activities such as bid defense meetings and project proposal development.

Qualifications:

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

  • Minimum 2 years of clinical trial management experience in the Asia-Pacific region, ideally in a CRO setting.

  • Experience managing studies in Cardiovascular, Renal, and Metabolic Diseases is required.

  • Strong written and verbal English communication skills.

  • Flexible, accountable, and adept at working in global, collaborative environments.

Why Join Medpace?

  • Office-based role with opportunities to work on internationally recognized trials.

  • Competitive salary and comprehensive benefits package.

  • Well-defined career development programs and mentorship.

  • Access to employee appreciation events, wellness programs, and professional training.

  • A culture that values expertise, innovation, and excellence in clinical trial execution.

About Medpace:
Medpace is a full-service clinical contract research organization (CRO) offering Phase I–IV development services across therapeutic areas including oncology, cardiology, CNS, endocrinology, and infectious diseases. Headquartered in Cincinnati, Ohio, with operations in 40+ countries and over 5,000 employees, Medpace is globally recognized for high-quality trial management.

Awards & Recognition:

  • Featured in Forbes’ America’s Most Successful Midsize Companies (2021–2024)

  • Repeated winner of CRO Leadership Awards for expertise, capabilities, and reliability

Estimated Salary: ₹15 – ₹22 LPA (based on role, experience, and CRO benchmarks)