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

Senior Project Manager, Site Activation Service

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:2016-11-25
  • 工作地点:上海
  • 招聘人数:若干人
  • 职位月薪:40-50万/年
  • 职位类别:生物工程/生物制药  

职位描述

职位描述:
About the Job:

Project Manager of Site Activation Service, lead core project team during study start-up phase and facilitate team’s ability to lead extended/complete project team. Depending on size and scope of project, this job duty may be performed in collaboration with a Project Director. Responsibilities include:

? Ensure effective cross-functional teamwork among project team members including both internal and external ancillary services. Serve as key client contact for assigned projects and escalation point for project issues. In collaboration with relevant departments, prepare and deliver presentations for new business as required.
? Lead implementation of Six Sigma initiatives on projects as applicable.
? Monitor project schedule and scope to ensure both remain on track. Initiate and implement appropriate actions.
? Proactively engage in both quality assurance and risk management activities to ensure project deliverables are met according to both Covance and client requirements.
? Initiate improvements to enhance the efficiency and the quality of the work performed on assigned projects.
? Accountable for budget across assigned project(s) including the control and minimizing of write-offs. Proactively identify out of scope activities and ensure necessary change orders are executed.
? Meet resource management and utilization targets for assigned staff, meet financial performance targets for the assigned projects and proactively participate in change control process both internally and externally.
? Ensure that all staff allocated to assigned project(s) adheres to professional standards and SOPs. Provide performance feedback of team members to respective supervisors.
? Define and manage project resource needs and establish succession plans for key resources.
? Create required project plans. Implement and monitor progress against project plans and revise as necessary. Responsible for appropriate issue escalation to CAIR program and/or appropriate stakeholders.
? Establish working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business.
? Prepare and actively participate as operational lead in internal project review meetings. Depending on size and scope of project, this job duty may be performed in collaboration with a Project Director.
? May have line management responsibilities for the training, utilization, development and performance review of assigned staff.
? Ensure lessons learned are implemented across projects currently being managed.
? Perform other duties as assigned by management.

Requirements:
? University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
? Minimum of seven (7) years relevant clinical research experience in a pharmaceutical company/CRO, including at least two (2) years of full project management responsibility, especially in the study start-up phase.
? In lieu of the above requirement, candidates with > five (5) years supervisory experience in a heath care setting and > five (5) years clinical research experience including two (2) years of project management experience (international clinical trial management experience preferred with solid knowledge of study start up) in the pharmaceutical or CRO industries will be considered.
? Thorough knowledge of project management processes, time and cost estimate development, ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs
? Fluent in local office language and in English, both written and verbal

Preferred:
? Masters or advanced degree.
? Experience in managing global projects with moderate financial value.

About Covance:
Covance is one of the world’s largest and most comprehensive drug development services companies, with more than 11,000 employees in 60 countries. We began operations Asia Pacific in 1988 and today have more than 1000 employees in 14 countries across the region. Through our discovery, nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.

Why Covance?
At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.

职能类别: 生物工程/生物制药

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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