Clinical Enrolment Manager 临床入组招募经理
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:2013-04-27
- 工作地点:广州
- 招聘人数:1
- 工作经验:三年以上
- 学历要求:本科
- 语言要求:英语熟练
- 职位类别:临床协调员 临床研究员
职位描述
Clinical Enrolment Manager
Responsibilities
Maintain updated patient database plus regular site contact and visits.
Collaborate and exchange information with site staff on a regular basis.
Collaborate and exchange information with CRAs (as appropriate) on a regular basis.
Identify opportunities for the LES service to be offered, through an appreciation of the sites? needs, awareness of the enrolment needs, information arising out of site meetings.
Contribute to the development and maintenance of an effective patient database.
Review patient notes, select and present high quality, patients to fulfil enrolment needs.
Review site screening records to identify potential subjects. Work with local centres to facilitate a patient referral process to main centres
Supply (and coordinate) information for brochures, newsletters, proposals and advertisements concerning the study recruitment.
Organise spirometry training and co-ordinate other appropriate trainings in co-operation with site staff to ensure continuous development.
Undertake the full range of duties relevant to the LES to ensure that performance meets and/or exceeds the enrolment for the study.
Maintain a positive, results-oriented work environment, building partnerships and modeling teamwork, communicating to the site staff in an open, balanced and objective manner.
Fixed period of support to the data cleaning activities
Experience - External:
Education:
To Degree level or equivalent nursing background
Minimum Work Experience:
Current study nurses with COPD background
CRAs with monitoring experience with COPD studies
Spirometry Technicians/Lung Function Technicians
Skills:
Excellent interpersonal, written and verbal communication skills including experience of making presentations.
Proficiency in Microsoft Word, Excel, power-point and Outlook.
Patient focussed and recruitment awareness, to be able to interact effectively.
A flexible attitude to work assignments and travel extensively within specified country
The ability to manage multiple and varied tasks with enthusiasm and prioritise workload with attention to detail.
ICH/GCP trained
Advantageous Experience:
Knowledge of the Pharmaceutical / Clinical Research industries
Experience in spirometry training
Experience in dealing with low recruiting sites
Experience with handling data queries and data clean up
Responsibilities
Maintain updated patient database plus regular site contact and visits.
Collaborate and exchange information with site staff on a regular basis.
Collaborate and exchange information with CRAs (as appropriate) on a regular basis.
Identify opportunities for the LES service to be offered, through an appreciation of the sites? needs, awareness of the enrolment needs, information arising out of site meetings.
Contribute to the development and maintenance of an effective patient database.
Review patient notes, select and present high quality, patients to fulfil enrolment needs.
Review site screening records to identify potential subjects. Work with local centres to facilitate a patient referral process to main centres
Supply (and coordinate) information for brochures, newsletters, proposals and advertisements concerning the study recruitment.
Organise spirometry training and co-ordinate other appropriate trainings in co-operation with site staff to ensure continuous development.
Undertake the full range of duties relevant to the LES to ensure that performance meets and/or exceeds the enrolment for the study.
Maintain a positive, results-oriented work environment, building partnerships and modeling teamwork, communicating to the site staff in an open, balanced and objective manner.
Fixed period of support to the data cleaning activities
Experience - External:
Education:
To Degree level or equivalent nursing background
Minimum Work Experience:
Current study nurses with COPD background
CRAs with monitoring experience with COPD studies
Spirometry Technicians/Lung Function Technicians
Skills:
Excellent interpersonal, written and verbal communication skills including experience of making presentations.
Proficiency in Microsoft Word, Excel, power-point and Outlook.
Patient focussed and recruitment awareness, to be able to interact effectively.
A flexible attitude to work assignments and travel extensively within specified country
The ability to manage multiple and varied tasks with enthusiasm and prioritise workload with attention to detail.
ICH/GCP trained
Advantageous Experience:
Knowledge of the Pharmaceutical / Clinical Research industries
Experience in spirometry training
Experience in dealing with low recruiting sites
Experience with handling data queries and data clean up
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)