Clinical Trial Assistant (CTA) 北京

月薪： 0.8-1.6万/月

该公司所有职位
  • 无工作经验
  • 招5人
  • 11-28 发布
  • 五险一金
  • 补充医疗保险
  • 补充公积金
  • 弹性工作
  • 定期体检
  • 出国机会
  • 年终奖金
  • 专业培训
  • 餐饮补贴

职位描述

职位描述： Duties and Responsibilities (including but not limited to):Supporting our Core Team at our PRA office, the Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials. Operating within the scope of the Clinical Development Plan, ICH-GCP guidelines and in accordance with the study protocol, local and international regulatory requirements and company procedures, the Clinical Trial Assistant (CTA) works to support the completion and coordination of various logistical and administrative tasks.The Clinical Trial Assistant’s (CTA) work is varied, fast-paced and quality focused. Typical duties will include supporting other members of the local study team, including Clinical Research Associates and Lead Monitors, collecting data required for regulatory submissions, document tracking (contracts, financial agreements, patient informed consent forms, insurance certificates) and managing the delivery of non-drug related study supplies. Maintaining constructive relationships with site staff (eg Investigators, Study Coordinators etc) as well as with colleagues within the organisation, the Clinical Trial Assistant is responsible for tracking site budget related matters, including processing invoices, tracking payments etc. The maintenance and updating of the Trial Master File (and preparation for relevant QC checks when applicable) also falls within the CTA’s remit.Functioning as a key component of the clinical study team, the Clinical Trials Assistant (CTA) may also be responsible for scheduling meetings, updating Excel trackers, coordinating the translation of site documents and providing ad-hoc support as appropriate.Education and Work Experience:To be considered for this position, you should have a bachelor degree (any discipline). In the case of having diploma as the highest education attained, you should have a few years of relevant industry experience.Ideally we would like minimum 1 year experience as CTA supporting clinical study projects. However, we would welcome candidates with other relevant industry experience to apply with us.Ability to read, write and speak basic English is essential, along with proficiency in the use of Microsoft Office suite. Document translation between English and Chinese is sometimes required.Demonstrable experience of working to high quality standards and resolving issues will also feature in your profile. The ability to effectively communicate with others and foster positive working relationships will guarantee success within this role. 职能类别： 临床研究员

联系方式

北京市朝阳区建国路91号金地中心B座917

公司信息

RPS Inc. is a next generation global CRO, headquartered in the United States with the operations in 45 countries throughout Americas (US, Canada, Latin America), EMEA and Asia Pacific regions. RPS provides comprehensive global Phase 1-4 clinical development solutions to the pharmaceutical, biotechnology and medical device industries. By combining an experienced clinical research operations infrastructure with the industry’s largest resourcing engines, RPS is uniquely positioned to offer our Clients both integrated and full service global outsourcing solutions. These solutions are powered by highly experienced and seasoned study teams providing innovative, cost-effective and high quality services. RPS Asia Pacific Headquarters is located in Beijing, China and we have operations in 11 Countries in Asia Pacific region. With the rapid organic expansion of RPS in China & Asia Pacific, we are continuously looking for the experienced industry talents to join us. Our specialized staff of consultants is eager to discuss your career plans. Tell us about yourself experience, so the appropriate consultant can contact you. RPS is sensitive to your daily responsibilities. Tell us EXACTLY how to contact you and we will. For your convenience, you can also submit your resume. We look forward to discussing the opportunities and benefits of employment with RPS! For more information, please visit our website www.rpsweb.com.

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