RWLPR Senior Site Manager 上海

月薪： 2-2.5万/月

该公司所有职位
  • 3-4年经验
  • 本科
  • 招若干人
  • 11-09 发布
  • 五险一金
  • 补充医疗保险
  • 补充公积金
  • 通讯补贴
  • 餐饮补贴
  • 交通补贴

职位描述

职位描述： PURPOSEEnsure clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements by engaging with assigned sites. Workload will include more complex projects. RESPONSIBILITIES ？May perform site selection, start-up/regulatory, initiation, monitoring and close out visits in accordance with contracted scope of work, using good clinical practices applicable regulations, SOPs and work instructions. ？Complete appropriate therapeutic, protocol and clinical research training to perform job duties. ？Work collaboratively with other functional groups such as Project Management, Regulatory Start-Up (RSU) and Epidemiology. ？ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. ？Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), Site Management Lead (SML) and/or line manager. ？ Independently execute assigned work efficiently and adhere to project timelines and financial goals; may provide Site and Patient Services performance metrics and make recommendations based on their findings. ？Drive the progress of assigned studies by documenting regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution. ？May assist in preparation for in-house audits and in creation of Corrective Action Plans (CAPAs). ？Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters, essential document collection and filing and other required study documentation. ？May mentor less experienced clinical staff, including demonstrating appropriate interactions with sites, performing accompanied remote monitoring visits and documentation, along with other monitoring activities. May act as point of contact for other Site Managers on the project. ？May assist Site Management Lead (SML) in the development of operational plans and project-specific scripts.REQUIRED KNOWLEDGE, SKILLS AND ABILITIES ？Strong knowledge of applicable clinical research regulatory requirements; i.e.,Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines ？Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint ？Strong written and verbal communication skills in applicable languages, and business level command of English ？Strong organizational, interpersonal and problem-solving skills ？Strong attention to detail ？Working time management skills ？Ability to establish and maintain effective working relationships with coworkers, managers and clients and site personnel at assigned sitesMINIMUM REQUIRED EDUCATION AND EXPERIENCE ？Bachelor’s Degree preferably in life science, and 3 years of monitoring experience; or equivalent combination of education, training and experiencePHYSICAL REQUIREMENTS ？Extensive use of telephone and face to face communication requiring accurate perception of speech ？Extensive use of keyboard requiring repetitive motion of fingers ？Regular sitting for extended periods of time ？May require occasional travel. 职能类别： 生物工程/生物制药 关键字： 英语流利，生命科学本科及以上学历，3年以上监测经验，或相当的教育/培训及经历

联系方式

枫林路388号枫林国际大厦A座3楼

公司信息

QuintilesIMS pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster. If that is your passion, we have a place for you.

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