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Clinical Trial Manager

Medpace
Medpace
2+ years
preferred by company
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Clinical Trial Manager – Navi Mumbai, India
Category: Clinical Trial Management
Experience Required: 2+ years in clinical trial management, preferably in CRO environment
Location: Navi Mumbai, India | Full-Time

About Medpace
Medpace is a leading global Contract Research Organization (CRO) providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. With over 30 years of experience, Medpace leverages local regulatory and therapeutic expertise to accelerate the development of safe and effective therapies. Headquartered in Cincinnati, Ohio, we employ 5,000+ professionals across 40+ countries, serving clients worldwide.

Role Overview
Medpace is expanding its Clinical Trial Management Group in Navi Mumbai, seeking skilled Clinical Trial Managers (CTMs). This role offers the opportunity to lead clinical trials across therapeutic areas including Cardiovascular, Renal, Metabolic, and Gastrointestinal studies. Candidates can continue working in their area of expertise or expand into new therapeutic domains.

Key Responsibilities

  • Lead end-to-end operational management of clinical trials, ensuring adherence to ICH/GCP guidelines, applicable laws, SOPs, and client-specific requirements.

  • Serve as the primary Sponsor contact for project-specific operational issues and study deliverables.

  • Maintain in-depth knowledge of study protocols, therapeutic areas, and indications.

  • Provide cross-functional oversight of internal project team members, ensuring all necessary training is completed.

  • Review and provide input on study protocols, edit check specifications, data analysis plans, and final study reports as applicable.

  • Develop operational project plans, conduct risk assessments, and implement mitigation strategies.

  • Manage vendors and site quality, including supervision of project Clinical Research Associates (CRAs) and monitoring of deliverables.

  • Track study milestones and ensure timely delivery of high-quality results.

Qualifications & Experience

  • Bachelor’s degree in Health Sciences, Life Sciences, or related field; Advanced degree preferred.

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

  • Proven experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal trials.

  • Strong communication skills, both written and spoken English.

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

Why Join Medpace?

  • Be part of a global CRO driving innovation and delivering meaningful impact in patient care.

  • Flexible work environment with structured career growth opportunities.

  • Competitive compensation and benefits packages, including PTO and wellness initiatives.

  • Recognition as a Forbes America’s Most Successful Midsize Company (2021-2024).

  • Award-winning culture with CRO Leadership accolades from Life Science Leader magazine.

  • Opportunities to collaborate on cutting-edge clinical trials with international teams and top-tier sponsors.

How to Apply
Submit your application via our portal with your CV and cover letter, highlighting relevant clinical trial management experience. Candidates who demonstrate experience in cardiovascular, renal, metabolic, or gastrointestinal trials will be prioritized.


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