Position: Clinical Project Management

Responsibilities :

Ÿ   Manage overall clinical projects from initiation, budget development, organization of project team, conduct of clinical project, quality operation, to the delivery of outcomes including CSR, timely and in compliance with applicable regulations 

Ÿ   Oversee performance of vendors including CROs, to ensure compliance with study protocol and in accordance with scope of work and timelines; identify areas of concern and escalate to CMO or CRO as appropriate

Ÿ   Provide operational inputs to study protocol

Ÿ   Assist in preparing CSR, annual safety reports, and other study documents

Ÿ   Effectively work with investigators, coordinators, and other site staffs

Ÿ   Assurance of regulatory compliance of investigational sites with company SOPs, EMA/FDA and ICH guidelines

Ÿ   Identify, select, and monitor performance of investigational sites for clinical studies; prepare accurate and timely visit reports from all site interaction visits

Ÿ   Manage/oversee investigational product (IP) accountability and reconciliation process

Qualification :

Ÿ   At least BS degree

Ÿ   Majored in related area such as medicine, pharmacy, pharmacology, veterinary medicine, biology or nursing

Ÿ   Holds of CRA experience, and at least 2 years of experience in PM

Ÿ   Strong communication skills in English both written and verbal

Ÿ   Experience in oncology therapeutic area is desirable

Additional information :

Ÿ   직책 및 직급: 직책 및 한글 직급 협의 후 결정 가능

Ÿ   급여 사항: 협의 후 결정

Ÿ   고용 형태: 정규직/경력직

Recruitment Process:

Ÿ   전형방법: 1차 서류전형/2차 & 3차 면접전형

Ÿ   제출 서류: 한글 이력서/자기소개서, 영문 이력서/자기소개서

Ÿ   채용 문의: hr@medirama.co.kr

Ÿ   기간: 2025년 2월 17일 – 2025년 3월 31일

Others

Ÿ   면접은 서류전형 합격자에 개별 통지합니다.

Ÿ   제출하신 서류는 일체 반환하지 않습니다

Ÿ   입사지원서 내용에 허위사실이 판명될 경우 입사가 취소될 수 있습니다.

기타 문의 사항은 반드시 E-mail로 문의바랍니다