Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully based in our Seoul, ASouth Korea 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. Oncology is one of Medpace’s leading therapeutic areas. We are involved in exciting programs in both solid tumors and hematologic indications. Our physicians are truly integrated with the project teams. We have developed strong relationships with key PIs throughout the world in many oncologic indications. In addition, our structure allows the clinical trial management team to focus on operational execution of the project, versus spending excessive time on project financial tracking.

The Clinical Trial Manager (CTM) position performs as project lead for multiservice clinical trials (some global in scope). The position interacts with sponsors and manages the timeline and all project deliverables. This role coordinates all services contracted for the study. CTMs are also responsible for leading a team of CRAs and managing project coordinators. • 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