R0000021608 外派CRA具体招聘要求有哪些？(R0000021608 外派CRA的工作需要怎样的学历？)

R0000021608 外派CRA具体招聘要求有哪些？(R0000021608 外派CRA的工作需要...)
外派CRA（临床研究助理）的招聘要求通常包括医学、药学或相关领域的学历背景，以及一定的临床试验或相关工作经验。对于R0000021608这一特定的职位，可能还会有特定的要求，如熟悉国际临床试验规范、良好的英语沟通能力，以及适应国际旅行和跨时区工作的能力和经验。外派CRA的工作内容包括监督临床试验的执行、确保试验的合规性、与研究团队沟通协调，以及撰写和审核临床数据和报告。

学历要求：本科
工作经验：2年
公司性质：外资（欧美）
公司规模：10000人以上  为了让HR同事及时与您联系以便获得更快的简历反馈，请您登录精鼎医药官方网站Jobs.Parexel搜索R0000021608投递您的简历进行职位申请。 At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out. As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home. 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.