Responisbilities :

Ÿ   Provide state-of-the-art medical knowledge input to all R&D projects (under consulting and co-development) as required

Ÿ   Provide medical input into documentations required for regulatory submissions

Ÿ   Provide medical interpretation of internal and external research data

Ÿ   Provide medical leadership as a Trial Physician and Medical Monitor

Ÿ   Provide medical advice and training to the other functional partners when necessary

Ÿ   Contribute to evaluation of in- and out-licensing opportunities and new project ideas

Ÿ   Contribute to the establishment and leveraging of an appropriate KOL network and interaction

Ÿ   Compose medical documentations on pharmaceutical R&D (CDP, TPP, Clinical study synopsis, clinical study report, investigator’s brochure)

Ÿ   Develop clinical development strategy in alignment with CDP & Business plan

Ÿ   Make timely decisions where there is no clear precedent and as a result is required to make new    approaches.

 

Qualification:

·        3 years or longer in pharmaceutical, biotech and/or academia after specialty board certificate

·        Pharma R&D in discovery, regulatory and/or clinical development experience preferred

·        Preferably, oncology experience, either in R&D or in medical/marketing in pharmaceutical industry, otherwise, in the hospital sector

·        Proficient English in written and spoken

·        Board certified specialist PhD (optional)

 

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   접수 방법 및 문의 사항: 온라인 지원, HR@medirama.co,kr  

 

Others

Ÿ   면접은 서류전형 합격자에 개별 통지합니다.

Ÿ   제출하신 서류는 일체 반환하지 않습니다

Ÿ   입사지원서 내용에 허위사실이 판명될 경우 입사가 취소될 수 있습니다.

Ÿ   기타 문의 사항은 반드시 E-mail로 문의바랍니다.