Clinical Research Associate (CRA) 北京

月薪： 0.8-1.6万/月

该公司所有职位
  • 无工作经验
  • 招1人
  • 11-09 发布
  • 五险一金
  • 补充医疗保险
  • 交通补贴
  • 餐饮补贴
  • 通讯补贴
  • 专业培训
  • 出国机会
  • 绩效奖金
  • 年终奖金
  • 弹性工作

职位描述

职位描述： OverviewAs a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.At PRA, borders do not create boundaries. PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals. Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community.Responsibilities1. Support study manager or S.CRA to prepare clinical trial, including study contracts development, study medication order, selecting potential investigator/site, developing protocol/ICF/ CRF, maintain filling system, according to Bayer’s strategy & timeline;2. Initiate, monitor and close-out sites ensuring their proper conduct according to relevant guideline, Bayer SOP, ICH-GCP and to ensure that data collected are an accurate representation of the facts (approximately 85% of the CRA’s time should be spent on monitoring). To set study commitments in association with the Study Manager and operate within them.3. Periodically report/update any study specific tracking systems of sites and update IMPACT database for responsible sites.4. Support study managers or S.CRA to manage and negotiate with external service providers.5. Join or aid in the training of Bayer and contract monitoring staff.6. Keep positive relationship with unit principle investigators and investigators.Qualifications / Experience1. Bachelor degree or above, major in clinical medicine or pharmacology2. More than 1 year experience in clinical research area is preferred3. Effective communication/negotiation skill4. Good written and oral English for communication within Bayer5. Good computer skill6. Team work spririt7. Be able to travel frequently 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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