MEDPACE에서는 사세 확장에 따라 아래와 같이 Clinical Trial Manager를 채용합니다.

- CTM - Oncology

- CTM - Infectious Disease and Neuroscience

MEDPACE 는 미국에 설립된 Global CRO로 본사는 미국 Cincinnati에 있으며 North/South America, Europe, Asia, the Middle East, Australia, Africa등 대부분의 국가에 지사를 두고 있습니다.

MEDPACE 한국 지사는 2012년 한국에 설립된 이후 현재까지 다양한 영역에서 Global 과제들을 전문적으로 수행하고 있습니다. 입사시 직원들에게 충분한 training기간을 통해 업무와 회사 생활에 적응할 수 있도록 지원하고 있으며, work & life balance를 통해 직원과 회사가 상생하는 것을 지향하고 있습니다.

관심있는 여러분의 많은 지원을 바랍니다.

Clinical Trial Manager

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;

- Manage study vendors where applicable; and

- Manage site quality and monitoring deliverables.

단체 상해보험/ 유연근무제/ 재택근무가능/ 명절상품권지급/ 경조휴가

Qualifications

- 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

- Prior CRO experience is preferred

- Excellent communication skills including good verbal and written English; and

- Flexible, accountable, and comfortable working in a global environment.

Email (SouthKoreaHR@medpace.com)로 영문이력서 (MS Word or PDF) 및 문의사항 발송

공고 관련 문의 : M.LauMeiSze@medpace.com