• 3-4年经验
  • 招1人
  • 英语精通
  • 11-09 发布
  • 五险一金
  • 补充医疗保险
  • 补充公积金
  • 员工旅游
  • 专业培训
  • 出国机会
  • 弹性工作
  • 定期体检

职位描述

职位描述: *Job Description?Deliver functional training, systems and/or partnership related training (depending on role and on assignments)The focus will be to deliver Clinical Operations training related courses.?Cross train on functional/system training materials as needed?Develop functional, systems and/or partnership related training materials as assigned.?Perform other training-related administrative tasks as assigned (e.g. production and communication of compliance metrics)?Perform partnership Training Lead role where assigned?Work with client related training professionals to provide access to client training programs, client training related systems, etc.?Attend (or where required, lead) internal training-related meetings.?Provide consultancy on training related matters.?Provide audit and inspection support, as assigned. This may include: providing assistance/advice for audit/inspection preparation; providing training-related or other input for audits and inspections as assigned; reviewing assigned audit/inspection responses.?Maintain a sound familiarity with PAREXEL systems and related processes.?Perform other assigned training, audit, inspection related tasks.?Remain informed about developments in relevant regulations and guidelines.?Share information in an open, balanced and objective manner with other PAREXEL professionals to maintain positive, results-orientated team environment.Identify improvement opportunities and act as a feedback loop related to training.*Job Qualifications?Strong interpersonal, verbal and written communication skills; good English.?Strong ability to deliver effective training where required?Strong ability to problem solve?Previous clinical trials experience preferable, with emphasis on GxP and compliance.?Client and first time quality focused approach to work.?Work with a sense of urgency.?Ability to work independently with oversight, take initiative, and have a flexible approach with respect to work assignments and new learning.?Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail and strong organizational skills.?Ability to work effectively in a matrix environment and to demonstrate and foster teamwork within the group as well as across the organization.?IT literate: experienced with Microsoft based applications, Excel, Word and general knowledge of personal computer functions knowledge of Clinical Trial Management Systems (CTMS), Electronic Document Management System (EDMS)?Ability to travel as needed for the position.?Ability to think and work globally and be culturally aware.?Ability to remain calm in times of stress?Good presentation skills and ability to deliver effective training where required.Need CRA, on-site monitoring experience. Must be able to deliver training in local language; but, also speak, read, write, English. 职能类别: 临床研究员 其他

联系方式

朝外大街乙12 號昆泰國際大廈15樓1505室

公司信息

精鼎医药研究开发(上海)有限公司(PAREXEL International),成立于1982年,是一家致力于药物临床试验研究的CRO (Contract Research Organization)集团公司。总部位于美国,分支机构遍布欧、美、亚、大洋四大洲,且于亚洲13个国家和地区设立了分支机构,致力深耕于当地。精鼎医药由一群具有丰富跨国性临床试验研发经验及专业知识的精英所组成,服务团队集合各种不同专业领域的人才。我们重视与客户的承诺,更重视人才的培育和养成,我们提供完整的教育训练、职涯规划、优于市场的薪资福利、良好工作环境,期许同仁与公司一同成长,迈向未来。 愿景(Vision): 创造一个在亚太地区具有国际竞争力的最精良CRO团队。 发展使命(Mission): 1.争取国际大药厂委托,执行符合国际水准的跨国性临床试验。 2.协助亚太生技及制药产业建立新药开发模式,以提升产品研发能力,幷促使产品国际化。 3.以提升临床试验品质为宗旨,拓展全球市场为目标,整合计算机及通讯科技,在国际上提供客户兼具成本效益及效率的临床试验数据处理中心。 4.建立一个以亚洲人种高发生率疾病的基因数据库,以提供国际性新药研发机构所须之基因信息,协助其缩短药物开发时程,幷提高研发成功率。 公司福利和人才培养计划: 保险类: 1. 社会保险(依照国家规定)及住房公积金; 2. 团体保险(包括寿险、意外暨医疗保险); 3. 补充医疗保险; 制度类: 1. 学习发展计划 (Learning & Development): 针对个别员工之专业及兴趣,设计符合其个人之生涯规划; 2. 完整的教育训练:每年公司均针对所有员工,提供完整之教育训练; 3. 顺畅的升迁管道及可转调其它部门;如有职缺,亦可申请调至海外各子公司; 请 / 休假制度: 1. 服务第一年即享有14天年假, 后续年休假天数则依据服务年资及公司制度而定; 2. 一年可享12天不扣薪病假; 3. 员工旅游, 年度体检; 精鼎医药将以培养国际性的人才为目标,欢迎具有国际观之人才加入。 应聘方法: 1.    在线投递; 2.    请登录我们的公司网站直接投您的简历(https://jobs.parexel.com/search-jobs) 我们在收到您的简历之后,会尽快与您联系。 谢谢!

猎才二维码