CRA II
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About this role
*본 포지션은 Core Team 소속으로, 모니터링 경력 2년 이상을 보유한 CRA 분들을 우선 검토하고 있습니다. Summary of Responsibilities: - Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. - Conducts site monitoring responsibilities for clinical trials according…
Excerpt only. The full posting is on the employer’s careers site.
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