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 current therapeutic area.

Responsibilities
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.

Qualifications
Bachelor’s 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 workplace;
Experience in Cardiovascular, Renal, Metabolic or Gastrointestinal related studies required;
Excellent communication skills including positive written and spoken English; and
Flexible, accountable and comfortable in working in a global environment.

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechno

📌 Clinical Trial Manager Navi Mumbai
🏢 Medpace
📍 Navi Mumbai