Training Specialist
精鼎医药研究开发(上海)有限公司
- 公司规模:10000人以上
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2017-10-19
- 工作地点:北京-朝阳区
- 工作经验:3-4年经验
- 学历要求:专业培训
- 语言要求:英语精通
- 职位月薪:1-1.5万/月
- 职位类别:临床研究员 其他
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.
*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
公司介绍
精鼎医药(Parexel International)是全球领先的药物研究合同委托机构(CRO),总部位于美国生物医药圣地马萨诸塞州的波士顿附近,在世界各地拥有71个办事处,约17,600 名员工,为超过100个国家的客户提供服务。
精鼎医药成立于1982年,在三十多年的历程中,一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商,并且取得了卓越成果。目前,我们能够提供全世界CRO领域全面的新药临床阶段研发服务,服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。
将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案,可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。
精鼎医药成立于1982年,在三十多年的历程中,一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商,并且取得了卓越成果。目前,我们能够提供全世界CRO领域全面的新药临床阶段研发服务,服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。
将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案,可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。
联系方式
- Email:tony.feng@parexel.com
- 公司地址:上海市浦东新区商城路506号新梅联合广场B座9层 (邮编:200120)