长沙招聘

Responsibility for Project Manager
? Ensure a professional, kind and efficient treatment of the research participants at CCBR.
? Ensure that the clinical studies are performed according to existing laws and regulations.
? Ensure that studies are performed according to CCBR standard procedures and quality regulations.
? Ensure that the clinical studies are performed according to the protocols.
? Ensure that patient data is handled according to the national Data Protection law.
? Ensure orderly and satisfactory working-conditions for the employees at the clinic.
? Ensure every single employee works efficiently and professionally.
? Ensure that every single employee is responsible for his/her working area, and is trained to obtain higher competences.
? Ensure that all staff involved in study has received the relevant training and new information before and during the study procedure.

Tasks for Project Manager
? Comply with ICH-GCP and local GCP and other relevant legislation
? Read and understand new protocols to be performed in the clinic
? Decide if a given trial can be performed in the clinic with success
? Plan the patient recruitment strategy for a given trial
? Plan and co-ordinate how study patients are informed about a given trial
? Plan and participate in audits from CCBR Global Study Management, sponsors and CRO’s.
? Handle the study medication
? Be in charge of informed consent process.
? Archive all relevant documents continuous in Investigator File
? Perform medical examinations at the clinic and fill in the relevant sections in the CRF and the patient journal.
? Go through and sign the CRF.
? Report side effects (AE) and follow up on these in close co-operation with the study responsible Study Nurse.
? Report serious adverse events (SAE) and follow up on these according to the protocol and local legislation.
? Evaluate and approve test results according to the protocol. Conclude on abnormal test results, and make sure adequate treatment is initiated.
? Manage the visits for the participants, both dropouts and final visits.
? Define the need for employees at the Clinical Department
? Assist the HR Manager in hiring employees for the Clinic Department
? Educate and train Clinical Department’s employees, in co-operation with the Global Study Management group in CCBR
? Co-ordinate the work of and supervise the employees for clinical studies.
? Initiate and plan arrangements with the purpose of increasing the solidarity between the employees and between different groups of employees in the clinic.
? Manage the daily activity at the clinic
? Plan efficient work flows for the employees of clinical department
? Work according to the agreed budget
? Plan the purchase needs for articles to the clinic within the budget with the approval from the Managing Director of CRC.
? Ensure that proper insurances are in place covering medical malpractice or the like
? Define and maintain the clinic safety policy according to national legislation.
? Go through the patient material in connection with enrolment for new studies.
? Complete ad hoc projects assigned by Managing Director of CRC, CCBR Beijing.

CCBR—全球***大SMO集团，于1992年在丹麦成立，在全球17个国家有40多个临床研究中心。CCBR一贯秉承质量为本的理念，提供一流的科学专业知识服务。
西斯比亚（北京）医药技术研究有限责任公司是CCBR在中国区的子公司，创办于2005年9月。西斯比亚（北京）是国际临床研究中心协会（SCRS）董事会成员、中国GCP联盟合作成员及中国SMO协作组***届理事会成员。
目前西斯比亚（北京）在中国拥有600多名CRC，覆盖全国近120个主要城市。

新候选人的隐私声明

当您提交信息以查询或申请临床与基础研究中心（北京）有限公司的职位空缺时，（地址：中国北京市昌平区生命园路 29 号中关村生命科学园生物科技创新大厦 C 座 1 楼，邮编：102206）（以下简称“CCBR”）我们将确保您的数据得到安全且保密的处理。
您的信息最初将由 CCBR 在中国的人力资源部同事以纸质和/或电子形式处理，以评估和管理您对本公司工作岗位的咨询或申请。我们不会将您的个人信息传输至中国境外地区。
如果您申请成功，则您的数据会作为新的任职记录的一部分保留下来；如果不成功，则您的信息会依照 CCBR 保留政策的要求保留 2 年，以备出现其他职位空缺。 此后，您的信息将被安全销毁。
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您有权要求 CCBR 以准确、最新且不具误导性的方式处理您的个人信息。此外，您有权访问并更正您的数据，请求删除，限制您的信息处理的各个方面，或要求以数字形式向您或第三方提供您的信息的副本。您可以通过向以下地址发送电子邮件来行使您的权利或要求进一步了解我们如何处理您的个人信息： AES_CCBR_HR_China@globalaes.com