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Clinical Trial Manager

Medpace
Medpace
2+ years
Not Disclosed
10 Jan. 22, 2026
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

Job Title: Clinical Trial Manager – Navi Mumbai
Location: Navi Mumbai, India
Employment Type: Full-time, Regular
Job ID: 11922


About the Role

Medpace, a global full-service Contract Research Organization (CRO), is seeking a Clinical Trial Manager (CTM) to oversee and manage clinical studies in Cardiovascular, Renal, Metabolic, or Gastrointestinal therapeutic areas. The CTM will ensure smooth day-to-day operations of clinical trials, maintaining compliance with ICH/GCP guidelines, sponsor expectations, and local regulatory requirements.


Key Responsibilities

  • Manage operational aspects of clinical trials, ensuring compliance with protocol, contract, ICH/GCP, and applicable laws and regulations.

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

  • Maintain in-depth knowledge of protocol, therapeutic area, and indication.

  • Provide cross-functional oversight of internal project team members, including training, deliverables, and timelines.

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

  • Develop operational project plans, including risk assessment and mitigation strategies.

  • Manage study vendors and oversee site quality, including supervision of Clinical Research Associates (CRAs).

  • Ensure timely and accurate completion of all clinical trial milestones.


Qualifications

  • Bachelor’s degree in Health, Life Science, or related field (Advanced degree preferred).

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

  • Experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal studies.

  • Excellent written and spoken English communication skills.

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


About Medpace

Medpace is a full-service CRO providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. With over 5,000 employees across 40+ countries, Medpace combines scientific expertise, local regulatory knowledge, and global reach to accelerate the development of safe and effective therapies.

Why Join Medpace?

  • Flexible work environment and competitive compensation packages

  • Generous PTO and structured career growth opportunities

  • Employee wellness initiatives and appreciation events

  • Recognition for leadership, quality, and reliability in clinical research

Medpace has been recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024) and continues to receive CRO Leadership Awards from Life Science Leader magazine.