Clinical Trial Manager-CVRM

Medpace is currently looking for Clinical Trial Manager/Director, Clinical Trial Management (Cardiovascular, Renal & Metabolic Disease (CVRM)) to lead global clinical research studies. This position is fully based in our Singapore office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials.

• 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;
• Manage study vendors where applicable; and
• Manage site quality and monitoring deliverables.

• 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;
• Manage study vendors where applicable; and
• Manage site quality and monitoring deliverables.