Clinical Research Associate (CRA)
Taipei, Taipei City, Taiwan 职位编号 82141BR 类别 Clinical Trials关于这个职位
What you’ll do:
-Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
-Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
-Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
-Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
-Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
-Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.
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