Remote CRA: Monitoring & Submissions for Global Trials

A health care company is seeking a Clinical Research Associate to manage clinical trials while ensuring compliance with regulations and ICH-GCP guidelines. Responsibilities include initiating, monitoring, and closing studies, preparing regulatory submissions, and supporting contracting processes. Required qualifications include a bachelor's degree in life sciences and at least two years of CRA experience. The role offers an attractive salary and a supportive team environment, with remote working options available. #J-18808-Ljbffr