CRA Trainee 临床监查员培训生
昆泰企业管理(上海)有限公司
- 公司规模:500-1000人
- 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:2017-06-10
- 工作地点:广州-越秀区
- 招聘人数:若干人
- 工作经验:2年经验
- 学历要求:本科
- 语言要求:英语 熟练
- 职位月薪:6000-9000/月
- 职位类别:临床研究员
职位描述
职位描述:
CRA Trainee项目是昆泰面对新人所设置的一个CRA专业人才培养项目,旨在通过昆泰的专业培训,培养输送合格的CRA到昆泰各个国际化项目中承担CRA的专业工作。
CRA Trainee在入职之初需要接受为期14周的全职培训。公司提供临床研究领域全球一流的培训资源,提供具有竞争力的薪资福利和专业的个人成长计划。
欢迎有医药相关教育背景,英语口语良好,勤奋工作者应聘!有少量CRA经验或临床研究领域相关经验者均可应聘!
面试合格者预计在2016年11月入职参加培训。
RESPONSIBILITIES
? Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
? Gain experience in study procedures by working with experienced clinical staff.
? Under close supervision, perform site selection (if applicable), initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practices.
? If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas to CRA for improving site recruitment plan in line with project needs to enhance predictability. Assist CRA in tracking subject site recruitment progress.
? Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
? Under close supervision, 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 as appropriate.
? Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution. Under close supervision may support start-up phase.
? Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
? Convey features and opportunities of study to site.
? Collaborate and liaise with study team members for project execution support as appropriate.
All responsibilities are essential to job functions unless noted as non-essential (N).
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
? Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
? Good written and verbal communication skills including good command of English language
? Good organizational and problem-solving skills
? Effective time management skills
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
? Bachelor's degree and above
? Less of 1 year CRA working experience
? Or less than 2 year related working experience
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CRA Trainee项目是昆泰面对新人所设置的一个CRA专业人才培养项目,旨在通过昆泰的专业培训,培养输送合格的CRA到昆泰各个国际化项目中承担CRA的专业工作。
CRA Trainee在入职之初需要接受为期14周的全职培训。公司提供临床研究领域全球一流的培训资源,提供具有竞争力的薪资福利和专业的个人成长计划。
欢迎有医药相关教育背景,英语口语良好,勤奋工作者应聘!有少量CRA经验或临床研究领域相关经验者均可应聘!
面试合格者预计在2016年11月入职参加培训。
RESPONSIBILITIES
? Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
? Gain experience in study procedures by working with experienced clinical staff.
? Under close supervision, perform site selection (if applicable), initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practices.
? If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas to CRA for improving site recruitment plan in line with project needs to enhance predictability. Assist CRA in tracking subject site recruitment progress.
? Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
? Under close supervision, 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 as appropriate.
? Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution. Under close supervision may support start-up phase.
? Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
? Convey features and opportunities of study to site.
? Collaborate and liaise with study team members for project execution support as appropriate.
All responsibilities are essential to job functions unless noted as non-essential (N).
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
? Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
? Good written and verbal communication skills including good command of English language
? Good organizational and problem-solving skills
? Effective time management skills
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
? Bachelor's degree and above
? Less of 1 year CRA working experience
? Or less than 2 year related working experience
职能类别: 临床研究员
公司介绍
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.
If that is your passion, we have a place for you.
联系方式
- Email:chinacampus@iqvia.com
- 公司地址:地址:span建国门外大街光华东里8号中海广场