Clnical Trial Assistant/临床试验助理 北京

月薪： 4.5-6千/月

该公司所有职位
  • 无工作经验
  • 招若干人
  • 英语良好
  • 12-11 发布
  • 五险一金
  • 补充医疗保险
  • 通讯补贴
  • 专业培训
  • 年终奖金
  • 弹性工作
  • 定期体检

职位描述

职位描述： Role PurposeThe Clinical Trials Assistant (CTA) is responsible for providing administrative and project tracking support to all staff involved in the project. The CTA is required to assist the Project Manager and study team with various tasks associated with running a large scale clinical trial. Generally, the CTA is responsible for assisting the project team in the ongoing execution and closeout of the trial.Reporting RelationshipsThe Clinical Trials Assistant reports to the Clinical Team Leader. This role will work closely with other clinical research staff including CRAs, SCRAs and with Project Managers across designated projects.Key accountabilities?Track the progress of a clinical trial including patient recruitment, trial supplies and trial documentation?Provide administrative support for designated clinical research personnel, including Project Managers, SCRAs and CRAs?Track and process invoices and authorised clinical trial payments to selected vendors and investigational sites, accurately and in a timely manner? Organise and schedule appointments/meetings, internally and externally, as necessary and prepare minutes of these meetings?Coordinate clinical trial supplies and documents to investigational sites, as directed?Act as a liaison between the CRA and investigator sites, as required?Assist in monitoring of timelines and resources? Assist in pharmacovigilance activities such as collating & tracking Serious Adverse Events (SAEs) and reporting to investigators?Regularly update project tracking tools and systemsStudy Design?Assist in the preparation of study documentation, forms and the development of administrative systems and processes?Assist in the distribution of study documents to investigators, site staff and the International Coordinating Centre?Assist in the planning and preparation of Investigator meetingsStudy Execution? Maintain up to date participating centre’s information (including all contact details, contracts and reports).?Assist with the collection, review and tracking of regulatory documents and endpoint data?Proactively identify study administrative issuesGeneral Clerical Duties? Accountable for the management of study materials and supplies - distribution, ordering, tracking, storage, reconciliation and destruction.?Provide administrative technical support to study team.?Assist with the preparation of study-related presentation materials?Responsible for the maintenance and filing of study administrative files?Assist project team with other study related activities such as organizing study meetings and scheduling travel, producing agendas and minutes for study-related meetings, assembling training and study materials, updating contact details, maintaining study documentation, assisting in the preparation of administrative documents and other tasks as required.?Assist in managing effective communication with the study team.?Participate in special projects to continuously improve processes, tools, systems and organisation.Personal Development:Mandatory attendance at core trainingParticipate in goal setting, performance management, review of position and planning and implementation of professional development activities.Participate in required meetings and workshopsOccupational Health and Safety?Comply with OH&S legislation and operate in accordance with established OH&S practice and procedures at The George Institute.?Promote and contribute to a safe, secure environment for staff and visitors.Skills, Knowledge and ExperienceBackground?Some understanding of medical terminology?Relevant experience in a clinical research environment?Basic knowledge of clinical trial processes and ICH/GCP guidelines desirableClerical?Strong general administration skills and experience.? Proficient in the use of the Microsoft Office suite of products, including Word, Excel, PowerPoint and Outlook and the Internet.GeneralExcellent interpersonal skills and the ability to work well and flexibly ie autonomously, in small teams and with a wide range of varying stakeholdersAbility to see the big picture, yet still focus on detailAbility to be flexible and adaptable in the face of changing organisational priorities and ambiguous environments.Strong focus on quality of work 职能类别： 临床协调员

联系方式

北京市海淀区知春路6号锦秋国际大厦B1802

公司信息

The George Institute China is a medical research institute, and a wholly-owned foreign enterprise, that was established as an affiliated partner with Peking University Health Science Centre in March 2007, whose registered name is Beijing George Medical Research Co. Ltd. The aim of the Institute is to promote high quality medical research through the conduct of randomised controlled trials and epidemiological studies with various government and non-government partners for the purpose of providing evidence-based approaches to improve the health of Chinese people.George Clinical is the clinical research delivery arm of the George Institute and manages phase I to phase IV clinical studies for both commercial and medical research organisations. George Clinical is recognized as a leading Clinical Research Organisation (CRO) bringing together medical and scientific expertise in the clinical trials area. George Clinical China is a wholly owned foreign enterprise and trades under the name George (Beijing) Clinical Research Co. Ltd.

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周边城市招聘： 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南

企业入驻日期： 2017-12-11

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