Clinical Research Associate - PRA Core Team 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
  • 年终奖金
  • 绩效奖金
  • 出国机会
  • 专业培训
  • 弹性工作
  • 定期体检
  • 餐饮补贴

职位描述

职位描述： Duties and Responsibilities (including but not limited to):Working fully as part of our Core Team and based at the PRA offices, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the site lifecycle, whilst working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard Operating Procedures.With full ownership of investigator sites for your assigned studies, your involvement begins at site feasibility stage, with responsibility for the successful management of the site right through to close-out. In addition to planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan, you will foster effective relationships with investigator site staff to ensure that key clinical metrics are met. This will involve establishing innovative ways of increasing site and patient recruitment. When issues do occur, the Clinical Research Associate proactively and promptly implements corrective action plans, and, when applicable, escalates issues to more senior members of the study team. You may also design and deliver training to site staff, when appropriate.Typical duties will likely include preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues that have occurred at your site. You will ensure the integrity of clinical data through your ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.Through your ability to operate as a key part of a global study team, you will play a fundamental role in our client’s drug development process.Education and Work Experience:The successful candidate for this role will be able to demonstrate prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.Ideally we would like for you to have at least 1 year of monitoring experience.It is essential that you have prior working knowledge of ICH-GCP guidelines and local and international regulatory requirements.Fluency in English is an absolute requirement, as well as an ability to communicate effectively with others and manage your time effectively. 职能类别： 临床协调员

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.

北京相关职位

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北京相关职位： 临床数据分析专员 临床数据管理专员 药理毒理研究员 制剂质量分析（QC) 制剂质量管理（QA） 生物分析高级研究员（TL） 化学新药研发项目经理（TL） 临床项目经理 高级临床监察员（CRA） 药学研究（韩语）

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： 2017-11-09

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