Clinical Research Manager 上海

月薪： 1.5-3万/月

该公司所有职位
  • 3-4年经验
  • 本科
  • 招2人
  • 11-09 发布
  • 五险一金
  • 定期体检
  • 补充医疗保险
  • 专业培训

职位描述

职位描述： Position Description:The Clinical Research Manager of Clinical Operation Division is responsible for leading, managing, mentoring and developing the clinical team. In addition to team management responsibilities, the manager plays an important role in directly/indirectly supervising clinical projects within his/her team, improving operational processes and implementing best practices to ensure on-time, on-budget performance.Responsibilities:1.Lead the team in line with company objectives and strategies.2.Set up the annual goals and resource/budget plans at department level with supervisor’s assistance to ensure profit and quality of the clinical projects.3.Recruit new staff and retain current staff according to the resource plan.4.Establish the career development plan for staff and provide opportunities/training/coaching to ensure adherence of staff to the qualification defined in corporate career ladder.5.Define/review/approve the KRAs and KPIs prepared by staff and conduct the performance evaluation in compliance with company standards.6.Identify and assign qualified staff for project team based on the project requirements and the development of the clinical team.7.Provide day-to-day technical and management guidance to deliver the clinical projects with quality in compliance with ICH-GCP and all applicable regulations.8.Supervise the project status (resource/budget/progress/issues) to ensure project milestones are met on time and within budget.9.Serve a subject expert and attend the training as a trainer.10.Play the role of SOP custodian.Qualifications:Education and Experience:1.A 4-year BS (Bachelor of Science) degree in Life Sciences or Pharmacy or a related field. Advanced degree is a plus.2.At least 4-year experiences as a clinical research associate in clinical research environment.3.At least 3-year experiences in project management.4.At least 1 year experience in people management.Skills/Competencies:1.Familiar with all clinical operation activities throughout an entire clinical trial.2.Excellent verbal and written communication skills.3.Good verbal and written English or other second language skills.4.Strong computer literacy e.g. MS word, Excel, PowerPoint, internet.5.Excellent organizational, record retention and time management skills.6.Excellent working knowledge of ICH-GCP, applicable law (local and country) and regulatory requirements.公司网站：http://www.apluscro.com/ 职能类别： 医药技术研发管理人员 临床协调员 关键字： 临床监查 试验管理 CRM 带薪年假 周末双休 话补 出差补贴

联系方式

上海市长宁区仙霞路317号2516室

公司信息

佳永医药咨询（上海）有限公司，是台湾佳生集团(PPC Group)旗下, 专责新药研发及临床试验的佳正国际股份有限公司(A+ Inc.) 在中国的分公司，台湾佳生集团成立于1997，是一家服务于亚太区制药企业，生物技术公司以及医疗器械公司的合同研究组织（CRO），主要提供新药研发的I – IV 期的临床试验服务。目前有员工580多人，主要分布在台北，首尔，东京和上海。 PPC集团网站 http://www.ppccro.com 佳永医药咨询（上海）有限公司网站：http://www.apluscro.com 公司地址：上海市长宁区仙霞路317号(远东国际广场B栋) 2516室

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