Position: CTA, Clinical Development

 

Responsibilities:

Ÿ   Assist updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.

Ÿ   Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.

Ÿ   Coordinate tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

Ÿ   Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

Ÿ   Accompany Clinical Development team members on site visits to assist with clinical monitoring duties upon completion of required training.

 

Qualifications:

Ÿ   Minimum one year clinical research experience strongly preferred. 

Ÿ   Written and verbal communication skills including good command of English language.

Ÿ   Effective time management and organizational skills.

Ÿ   Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Ÿ   Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.

Ÿ   Knowledge of applicable protocol requirements as provided in company training knowledge.

 

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 담당: 온라인 지원, HR@medirama.co,kr  

Ÿ   마감일: 2024년 8월 31일

 

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.