CRA, 2년 이상
[담당업무]
- CRAs primary responsibility is to build relationships with Principal Investigators, study co-ordinators, pharmacists,
  and all relevant site trial personnel to ensure the efficient, expedited, and smooth management of project.
- Work in a timely manner in accordance with the agreed budget, under the supervision of the project manager(PM)
- Communicate with the PM, other CRAs, Sponsor and site staff as appropriate
- Conduct initiation, interim monitoring, and close-out visits
- Undertake monitoring visit within the correct timeline and ensure with report that all activities
  such as source data verification and drug accountability are completed
[필수사항]
- 임상시험 1~4상 모니터링 경력(허가임상 경험 필수), 2년 이상
- 전공: 간호학, 약학, 수의학, 자연과학, 생명과학, 보건계열 관련 전공자
- 허가 임상시험 연구 경험, Oncology 임상시험 경험자 우대
[우대사항]
- IIT 연구 경험, Oncology 임상시험 경험자 우대
- 빠른 입사 가능자