Associate Manager, ClinOps
科文斯医药研发(上海)有限公司
- 公司规模:1000-5000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:2017-11-29
- 工作地点:北京-朝阳区
- 工作经验:5-7年经验
- 学历要求:本科
- 语言要求:英语熟练
- 职位月薪:1.5千以下/月
- 职位类别:临床研究员
职位描述
职位描述:
-Responsible for the supervision of assigned direct reports
-Responsible for detailed performance review and management of assigned direct reports including: Annual Performance Management and Development (PMD), Individual Development Plan (IDP), Line of Sight Goals and “Shoves & Tugs”
-Responsible for appropriate management and resolution of performance issues
-Measure performance indicators for assigned staff within Clinical Operations.
-Escalate potential individual training needs and assist in the conduct of training and development efforts, regionally
-Conduct Evaluation and Quality Control Visits for Clinical Operations staff
-Effectively communicate management strategies, policies and procedures in conjunction with leadership teams
-Develop and maintain effective relationships with management team to manage Clinical Operations staff in a matrix environment
-Maintain good working relationships with internal and external clients to ensure opportunity for acquiring additional new business
Criteria:
*University/college degree – life sciences preferred or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
*In lieu of this required educational background the following relevant work history may be considered: Minimum of two (2) years supervisory experience in a health care or clinical research setting and Minimum of six (6) years relevant clinical research experience in a pharmaceutical company/CRO
*Relevant clinical research experience in a pharmaceutical company or CRO:
?Individual is proficient with on site monitoring activities (including pre-study, initiation, routine monitoring and closeout visits)
?Minimum of four (4) years relevant clinical research experience in a pharmaceutical company/CRO
?Thorough knowledge of drug development process
?Thorough knowledge of relevant SOPs, ICH, and GCP guidelines
*Relevant supervisory experience
?Some experience as a Line Manager or Project Manager preferred
?Demonstrated ability to lead by example and to encourage team members to seek solutions
?Proven interpersonal skills
?Demonstrated ability to successfully participate as a member of a project team
?Demonstrated ability to successfully manage multiple competing priorities
?Excellent planning and organizational skills
?Excellent oral, written and presentation skills
-Responsible for the supervision of assigned direct reports
-Responsible for detailed performance review and management of assigned direct reports including: Annual Performance Management and Development (PMD), Individual Development Plan (IDP), Line of Sight Goals and “Shoves & Tugs”
-Responsible for appropriate management and resolution of performance issues
-Measure performance indicators for assigned staff within Clinical Operations.
-Escalate potential individual training needs and assist in the conduct of training and development efforts, regionally
-Conduct Evaluation and Quality Control Visits for Clinical Operations staff
-Effectively communicate management strategies, policies and procedures in conjunction with leadership teams
-Develop and maintain effective relationships with management team to manage Clinical Operations staff in a matrix environment
-Maintain good working relationships with internal and external clients to ensure opportunity for acquiring additional new business
Criteria:
*University/college degree – life sciences preferred or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
*In lieu of this required educational background the following relevant work history may be considered: Minimum of two (2) years supervisory experience in a health care or clinical research setting and Minimum of six (6) years relevant clinical research experience in a pharmaceutical company/CRO
*Relevant clinical research experience in a pharmaceutical company or CRO:
?Individual is proficient with on site monitoring activities (including pre-study, initiation, routine monitoring and closeout visits)
?Minimum of four (4) years relevant clinical research experience in a pharmaceutical company/CRO
?Thorough knowledge of drug development process
?Thorough knowledge of relevant SOPs, ICH, and GCP guidelines
*Relevant supervisory experience
?Some experience as a Line Manager or Project Manager preferred
?Demonstrated ability to lead by example and to encourage team members to seek solutions
?Proven interpersonal skills
?Demonstrated ability to successfully participate as a member of a project team
?Demonstrated ability to successfully manage multiple competing priorities
?Excellent planning and organizational skills
?Excellent oral, written and presentation skills
职能类别: 临床研究员
关键字: 临床
公司介绍
LabCorp是全球顶尖的生命科学公司,科文斯作为LabCorp旗下的药物研发部门,肩负着改善人类健康与生命的共同使命。科文斯的实验室和设施遍布全球,在世界范围内拥有超过26000名员工,卓越的研发能力和强大的人才资源奠定科文斯在医药研发行业的领先地位。截止到2020年,科文斯中国团队共参与了近100个获得上市许可的新药研发,积极支持超过50个免疫肿瘤药物的研发项目,是服务***面的药物研发公司。
欢迎加入科文斯中国团队,我们提供优厚的薪酬、完善的培训以及灵活的办公方式。也请关注“科文斯招聘”微信公众号,通过移动端迅速查询热招职位并投递申请,与我们并肩实现#CovancePotential。
欢迎加入科文斯中国团队,我们提供优厚的薪酬、完善的培训以及灵活的办公方式。也请关注“科文斯招聘”微信公众号,通过移动端迅速查询热招职位并投递申请,与我们并肩实现#CovancePotential。
联系方式
- Email:yuanxin.fang@covance.com
- 公司地址:地址:span浦东新区伽利略路338号9号楼