上海 [切换城市] 上海招聘上海生物/制药/医疗器械招聘上海生物工程/生物制药招聘

Clinical Operations Manager

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:2017-03-08
  • 工作地点:北京-朝阳区
  • 招聘人数:若干人
  • 学历要求:本科
  • 语言要求:英语 熟练 普通话 精通
  • 职位月薪:2.5-5万/月
  • 职位类别:医药技术研发管理人员  生物工程/生物制药

职位描述

职位描述:
People Responsibilities:
Direct Reports: Between 10 and 20 Clinical Operations Staff, dependent upon business need
Indirect Reports: None

Job Duties:
A. GCP and Quality Oversight:
? Has GCP oversight of direct reports by ensuring GCP training is executed, understood and implemented
? Identify and escalate GCP issues identified through regular interactions with direct reports and conduct of Accompanied Field Visits
? Ensures training record compliance with training matrix and ensures training records are up to date
? Provide input to relevant SOPs and standard plans/templates for use by Project Management and Clinical Operations staff
? Assist with on-boarding of new direct reports ensuring GCP training before monitoring begins
? Hold Clinical Operations staff accountable for GCP issue escalation to the management team, the sponsor and QA, as appropriate
? Hold Clinical Operations staff accountable for quality and compliance with project plan and adherence to contract obligations in Source Data Verification, Monitoring Visit cycles, Trip Report quality and on time deliverables
? Coach Clinical Operations staff to own effective Investigator relations and Investigator oversight at the local level
B. Productivity and Financial Management:
? Communicate status of assigned workload for metric reporting
? Perform weekly review of direct report billable hours and associated utilization per the quarterly and annual budget plan, and escalation of outliers to management team for mitigation
? Escalates available workload hours, in context of project allocation, supply and demand, to management team
? Adheres to global tools for monitoring and utilization forecasting
? Engage in Resource management activities for direct reports
? Assist with staff recruitment through screening and interviewing
? Financial authority in accordance with current signature approval matrix
? Accountable for expense management, expense report approval and compliance with Travel Policy of direct reports
? Liaise with internal and external customers in relevant process improvement initiatives, including Six Sigma
? Encourages use of standardized processes and tools in alignment with associated policies to ensure efficiency and productivity
? Schedule Accompanied Field Visits to ensure costs are in alignment with regional budget
Utilization of direct reports in conjunction with the Country Lead and Management Team.
C. Principal Contacts and Scope of Communications:
? Clinical Operations Staff
? Country Lead
? Senior Directors
? Project Directors
? Project Managers
? Regulatory Department
? Quality Assurance Department
? Finance Department
? Human Resources Department
? Legal Department

Requirements:
A. Travel: Yes
? 30-50% travel by plane and car as required with overnight and domestic/potential international travel
? Ability to drive and have a valid driver’s license as appropriate per country travel norms
B. Language Skills:
? Speaking: English and Local Language required
? Writing/Reading: English and Local Language required
C. Education/Qualifications
? 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 three (3) years supervisory experience in a health care or clinical research setting and
? Minimum of seven (7) years relevant clinical research experience in a pharmaceutical company/CRO
Preferred:
? Masters or other advanced degree
D. Experience
? 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 five (5) 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
? Minimum of 1 year as a Line Manager or Project Manager required
? 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: 医药技术研发管理人员 生物工程/生物制药

关键字: covance 科文斯 生物制药 生物医药 COM Clinical Operations Manager

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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。

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