임상팀장 (차장-과장급)
- Company
- 유명상장제약회사
- Position
- 임상팀장 (차장-과장급)
- Status
- OPEN
유명 상장 제약회사에서 다음과 같이 “임상팀장” 인재를 찾습니다.
* Job Title : 임상팀장
* Position : 차장 - 과장
* Gender : Male or Female
* Location : 서울 강남
* Job Title : 임상팀장
* Position : 차장 - 과장
* Gender : Male or Female
* Location : 서울 강남
[RESPONSIBILITIES]
- Set-up project direction to achieve clinical research duties
- Responsible for budget and control of CRA project
- Perform site selection, initiation, monitoring and close-out visits in accordance with scope of work and good clinical practice
- Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution
- Generate and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation
- May provide assistance to more less experienced clinical staff
- Set-up project direction to achieve clinical research duties
- Responsible for budget and control of CRA project
- Perform site selection, initiation, monitoring and close-out visits in accordance with scope of work and good clinical practice
- Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution
- Generate and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation
- May provide assistance to more less experienced clinical staff
[QUALIFICATIONS]
- Pharmacist or Registered Nurse preferred
- Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- In depth therapeutic and protocol knowledge
- Excellent organizational and problem-solving skills
- Effective time management skills
- Ability to manage competing priorities
- Ability to establish and maintain effective working relationships
- 팀장 역할 경험자 선호
- Pharmacist or Registered Nurse preferred
- Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- In depth therapeutic and protocol knowledge
- Excellent organizational and problem-solving skills
- Effective time management skills
- Ability to manage competing priorities
- Ability to establish and maintain effective working relationships
- 팀장 역할 경험자 선호
Those who are interested in this opportunity, please submit your Resume in MS Word Format by email urgently. Only qualified candidates will be contacted for interview. All resumes not contacted will be kept in DB confidentially for future positions.
Kyung Jin KIM
CEO & Executive Search Consultant
Exdigm Inc.
Phone: 070-8260-3646
Mobile: 010-8722-1272
Email: ceo@exdigm.com exdigm@naver.com
