精神病学和行为科学系人类神经回路(HNC)项目正在寻找一名助理临床研究协调员，以执行与临床研究相关的职责，探索氯胺酮在各种神经精神疾病(包括癫痫患者)中的机制。具体来说，该职位将涉及收集临床数据和协调正在进行的神经精神疾病临床研究项目。这将包括收集认知和生理评估以及神经成像(将提供培训)。我们的使命是以同情心服务我们的患者，与跨学科科学家和社区伙伴合作，并领导创新的高质量研究，加速和改变严重精神疾病的治疗。助理临床研究协调员将与主要研究者和临床研究经理密切合作并接受其监督。

我们的实验室正在寻找一名对精神健康有热情的团队成员，希望推动快速反应治疗的创新，并深入了解各种神经精神疾病(包括癫痫)的大脑基础。我们致力于打造一个包容、有趣、支持、跨学科和引人入胜的工作场所。我们鼓励保持健康的工作与生活平衡，提供学习新技能的机会，并为此提供时间和支持。我们强烈鼓励您申请并了解更多!

职责包括:

• 安排及/或致电预约当事人;与与会者联系，提出提醒或其他要求。

• 准备，分发和处理问卷。

• 履行文书职责，准备法规文件。维护所有的表格和文件，包括同意书和主体日志。将所有适当的信件归档。

• 协助筛选、招募和获得研究参与者的同意。根据需要，审查医疗记录和/或进行电话或面谈以收集数据。

• 管理标准的研究问卷和测试，评分测试测量和问卷，并为计算机输入编码数据。对表格、测试和其他测量进行定量审查，以确保完整性和准确性。

• 根据指导从源文件提取数据进行研究研究。收集资料，完成病例报告表。

• 经过适当的培训/认证后，根据方案对患者进行基本的测量和测试，如认知任务、获取生命体征和心电图。根据研究方案收集神经影像学或研究标本。

• 协助处理取出的患者电极和组织处理。根据明确的要求，准确地准备，加工和运输样品。

• 订购和维护设备和用品。

• 处理受试者完成试验活动后的研究补偿支付和感谢信。根据需要，协助完成学习后的活动。

• 协调由独立评估者进行的评估。

• 协调独立评价者的质量控制季度会议。

• 监督内部临床研究，并向每季度的临床运营会议提交监督表格。

• 领导每周的学习会议。

• 处理咨询发票。

*所列出的工作职责是本职位分类中各职位所执行的工作的典型例子，不包含或解释为所有职责、任务和职责的综合清单。在不改变工作的一般性质和范围或责任水平的情况下，具体的职责和职责可能会根据部门或项目的需要而变化。员工也可以执行其他分配的任务。

所需的资格:

• 优秀的写作和沟通能力。

• 熟悉常见的生物安全程序。

• 心理学，人类生物学或相关领域的学士或学士学位。

• 有临床研究经验，尤其是对精神卫生患者的研究经验(但不是必需的)。

• 具备临床研究药物临床试验管理规范(或愿意学习)知识。

• 有组织工作和多任务处理能力。

• 有维护临床研究资料夹和使用电子记录方法的经验(或愿意学习)。

• 熟练的计算机技能和使用办公软件和电子邮件的经验。
  

• 成功地完成日常工作。

• 较强的组织能力和注意细节。

• 优秀的客户服务和人际交往能力。

• 优先级和多任务处理能力。

了解更多：

https://medcareers.stanford.edu/job/stanford/assistant-clinical-research-coordinator/27938/65506850816

The Human Neural Circuitry (HNC) Program in the Department of Psychiatry and Behavioral Sciences is seeking an Assistant Clinical Research Coordinator to perform duties related to clinical research exploring the mechanisms of ketamine in various neuropsychiatric disorders, including in epilepsy patients. Specifically, the position will involve collection of clinical data and the coordination of ongoing clinical research projects for neuropsychiatricdisorders. This will include collection of cognitive and physiological assessments and neuroimaging (training will be provided). Our mission is to serve our patients with compassion, to collaborate with interdisciplinary scientists and community partners, and to lead innovative high-quality research studies that accelerate and transform treatments for severe mental illness. The Assistant Clinical Research Coordinator will closely work with and be under the supervision of the principal investigator and clinical research manager.

Our lab is seeking a team member who is passionate about mental health and wants to drive innovation toward rapid-acting treatments and insights into the brain basis of various neuropsychiatric disorders, including epilepsy. We are committed to an inclusive, fun, supportive, interdisciplinary, and engaging workplace. We encourage a healthy work-life balance, opportunities to learn new skills, and provide time and support to make this possible. We strongly encourage you to apply and find out more!

This is an on-site role.

Duties include:

• Schedule and/or call subjects for appointments; contact participants with reminders or other requirements.

• Prepare, distribute, and process questionnaires.

• Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence.

• Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to gather data, as needed.

• Administer standard study questionnaires and tests, score test measurements and questionnaires, and code data for computer entry. Perform quantitative review of forms, tests, and other measurements for completeness and accuracy.

• Extract data from source documents for research studies as directed. Collect data and complete case report forms.

• Perform basic measurements and tests on patients according to protocol, such as cognitive tasks, obtaining vital signs and EKG, after appropriate training/certification. Collect neuroimaging or study specimens according to protocol.

• Assist in handling explanted patient electrodes and tissue processing. Prepare, process, and ship specimens/samples accurately under well-defined requirements.

• Order and maintain equipment and supplies.

• Process study compensation payments and thank-you letters to subjects upon completion of trial activities. Assist with post-study activities, as needed.

• Coordinate assessments performed by independent evaluators.

• Coordinate quality control quarterly meetings for independent evaluators.

• Monitor internal clinical studies and present monitoring forms to the quarterly clinical operations meetings.

• Lead the study-specific weekly meeting.

• Process consultation invoices.

• *The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

DESIRED QUALIFICATIONS:

• Excellent writing and communication skills.

• Knowledge of common biosafety procedures.

• BA/BS in Psychology, Human Biology, or a related field.

• Clinical research experience, particularly with mental health patients (but not required).

• Knowledge of good clinical practice (GCP) in clinical research (or willing to learn).

• Ability to organize work and multi-task.

• Experience with maintenance of clinical study binders and interface with electronic record-keeping methodologies (or willing to learn).

• Proficient computer skills and demonstrated experience with office software and email applications.

• Demonstrated success in following through and completing routine tasks.

• Strong organizational skills and attention to detail.

• Excellent customer service and interpersonal skills.

• Ability to prioritize and multi-task.

EDUCATION & EXPERIENCE (REQUIRED):

Two-year college degree and one year of relevant experience or an equivalent combination of experience, education, and training.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

General knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

Working toward professional certification(s) for clinical research.

了解更多：

https://medcareers.stanford.edu/job/stanford/assistant-clinical-research-coordinator/27938/65506850816

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