Clinical Trial Assistant
丘以思（上海）医药信息咨询有限公司
- 公司规模：50-150人
- 公司性质：外资(欧美)
- 公司行业：制药/生物工程
职位信息
- 发布日期：2013-09-17
- 工作地点：广州
- 招聘人数：1
- 学历要求：本科
- 语言要求：英语良好
- 职位类别：临床协调员 其他
职位描述
Overall Job Purpose:
The Clinical Trial Assistant (CTA) has the responsibility for the successful delivery of the assigned clinical research tasks within his/her defined territory under the supervision of the (A)CRM/(A)CRD.
1. Key Accountabilities
1.1 Project Related Accountabilities
? Provide general administrative support to the clinical study team and assistance to Project Managers (PMs).
? Assist the clinical study team in completion of all required tasks to meet departmental and project goals.
? Support the clinical study team with ongoing conduct of studies.
? Be familiar with ICH-GCP, appropriate regulations, relevant SOPs and internal tracking systems.
? Be familiar with the roles and responsibilities of the CRA including site visits, if appropriate.
? Assist project teams with study-specific documentation and guidelines as appropriate.
? Set up, organize and maintain clinical study documentation (e.g., Trial Master Files, CRFs, etc.) including preparation for internal/external audits, final reconciliation and archival.
? Process Data Collection Forms, i.e., logging in, tracking and quality controlling as appropriate for the study.
? Coordinate ordering/dispatch and tracking of project materials (e.g., CRFs, diary cards, lab supplies, IP supplies) as appropriate.
? Assist in the tracking and distribution of safety reports.
? Coordinate document translation, if required.
? Attend project team meetings and generate meeting minutes.
? Assist in the production of slides, overheads, etc., as needed for project, departmental, sponsor and/or business development presentations.
? Other duties as assigned by PMs/CRMs/CRDs.
1.2 Relationship Management
Be responsible for contributing to the establishment of a strong team spirit.
2. Job Requirements:
? A Bachelor/Master degree in a scientific or health care discipline.
? Knowledge of international standards GCP/ICH and local regulations
? Skillful in Microsoft Office (Word、Excel、PowerPoint, ect)
? Proficiency in English communication
The Clinical Trial Assistant (CTA) has the responsibility for the successful delivery of the assigned clinical research tasks within his/her defined territory under the supervision of the (A)CRM/(A)CRD.
1. Key Accountabilities
1.1 Project Related Accountabilities
? Provide general administrative support to the clinical study team and assistance to Project Managers (PMs).
? Assist the clinical study team in completion of all required tasks to meet departmental and project goals.
? Support the clinical study team with ongoing conduct of studies.
? Be familiar with ICH-GCP, appropriate regulations, relevant SOPs and internal tracking systems.
? Be familiar with the roles and responsibilities of the CRA including site visits, if appropriate.
? Assist project teams with study-specific documentation and guidelines as appropriate.
? Set up, organize and maintain clinical study documentation (e.g., Trial Master Files, CRFs, etc.) including preparation for internal/external audits, final reconciliation and archival.
? Process Data Collection Forms, i.e., logging in, tracking and quality controlling as appropriate for the study.
? Coordinate ordering/dispatch and tracking of project materials (e.g., CRFs, diary cards, lab supplies, IP supplies) as appropriate.
? Assist in the tracking and distribution of safety reports.
? Coordinate document translation, if required.
? Attend project team meetings and generate meeting minutes.
? Assist in the production of slides, overheads, etc., as needed for project, departmental, sponsor and/or business development presentations.
? Other duties as assigned by PMs/CRMs/CRDs.
1.2 Relationship Management
Be responsible for contributing to the establishment of a strong team spirit.
2. Job Requirements:
? A Bachelor/Master degree in a scientific or health care discipline.
? Knowledge of international standards GCP/ICH and local regulations
? Skillful in Microsoft Office (Word、Excel、PowerPoint, ect)
? Proficiency in English communication
公司介绍
Clinipace Clinical Research，一个基于科技的全球性全方位服务的数字化合同研究组织（dCRO）。我们开创性的开发了依靠技术创新的CRO服务模式，以满足风险投资支持的，中型的战略性制药，生物技术公司以及医疗器械公司的研发需求。
借助于我们专有的TEMPO?电子化临床试验平台，我们的专家团队用他们丰富的治疗领域知识和见解来帮助生命科学公司制定和执行注册策略，临床开发和上市后研究，以确保药物和医疗器械开发计划的成功。
Clinipace的***目标就是通过开拓创新的技术继续坚定不移地致力于客户的成功，以最具性价比的全球性解决方案服务客户，提供高透明度，灵活和高质量的服务。
我们已经开展了超过1500个全球性的临床研究，完成了超过300个注册和开发策略制定项目。治疗领域涵盖如心血管和代谢，中枢神经系统，皮肤，消化，免疫，感染，***，肿瘤，呼吸，风湿和疫苗（和其他细胞和组织疗法）。
Clinipace刚刚庆祝了他们的10周年。如今，Clinipace其总部设在美国北卡罗莱纳州的Research Triangle Park，为横跨4大洲的27个国家提供服务。
因为对更高的数据准确度，经济高效的解决方案和更低的研发成本的需求在不断的增加，Clinipace还在持续的在全球扩张。
最后, Clinipace以正直透明、追求卓越绩效的企业文化邀请您的加入.
公司主页：*************************
最后, 丘以思以正直透明、追求卓越绩效的企业文化邀请您的加入.
应聘邮箱：kding@clinipace.com
借助于我们专有的TEMPO?电子化临床试验平台，我们的专家团队用他们丰富的治疗领域知识和见解来帮助生命科学公司制定和执行注册策略，临床开发和上市后研究，以确保药物和医疗器械开发计划的成功。
Clinipace的***目标就是通过开拓创新的技术继续坚定不移地致力于客户的成功，以最具性价比的全球性解决方案服务客户，提供高透明度，灵活和高质量的服务。
我们已经开展了超过1500个全球性的临床研究，完成了超过300个注册和开发策略制定项目。治疗领域涵盖如心血管和代谢，中枢神经系统，皮肤，消化，免疫，感染，***，肿瘤，呼吸，风湿和疫苗（和其他细胞和组织疗法）。
Clinipace刚刚庆祝了他们的10周年。如今，Clinipace其总部设在美国北卡罗莱纳州的Research Triangle Park，为横跨4大洲的27个国家提供服务。
因为对更高的数据准确度，经济高效的解决方案和更低的研发成本的需求在不断的增加，Clinipace还在持续的在全球扩张。
最后, Clinipace以正直透明、追求卓越绩效的企业文化邀请您的加入.
公司主页：*************************
最后, 丘以思以正直透明、追求卓越绩效的企业文化邀请您的加入.
应聘邮箱：kding@clinipace.com
联系方式
- Email：kding@clinipace.com
- 公司地址：地址：span广州