Work as Clinical Trial Manager at Medpace

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

Post : Clinical Trial Manager

Job Summary
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Navi Mumbai, India Office. Clinical Trial Managers with expertise in Cardiovascular, Renal, Metabolic or Gastrointestinal related are welcome to continue to work in their area of expertise or to expand to a new therapeutic area.

Job Description
• Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations;
• Serve as primary Sponsor contact for operational project-specific issues and study deliverables;
• Maintain in depth knowledge of protocol, therapeutic area, and indication;
• Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
• Develop operational project plans;
• Manage risk assessment and execution;
• Responsible for management of study vendor; and
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.

Candidate Profile
• Bachelors degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred;
• At least 2 years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
• Experience in Cardiovascular, Renal, Metabolic or Gastrointestinal related studies required;
• Excellent communication skills including good written and spoken English; and
• Flexible, accountable and comfortable in working in a global environment.

Additional Information
Experience : 2 years
Qualification : Bachelor’s degree in a health or life science
Location : Navi Mumbai, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Trial Management
End Date : 10th December 2026