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.

• Bachelor’s degree or above in health/life science related field; • At least two years of clinical trial management experience in the Asia Pacific region; indications of interest a plus • Excellent communication skills including good verbal and written English; and • Flexible, accountable, and comfortable working in a global environment.

• Prior CRO experience is preferred