PROJECT COORDINATOR(职位编号:2027196)
GE医疗集团
- 公司规模:5000-10000人
- 公司行业:医疗设备/器械
职位信息
- 发布日期:2015-03-02
- 工作地点:北京
- 招聘人数:1
- 工作经验:1年
- 学历要求:本科
- 语言要求:英语良好
- 职位月薪:面议
- 职位类别:项目执行/协调人员
职位描述
Business Segment
Healthcare Science Technology
About Us
GE (NYSE: GE) works on things that matter. The best people and the best technologies taking on the toughest challenges. Finding solutions in energy, health and home, transportation and finance. Building, powering, moving and curing the world. Not just imagining. Doing. GE works. For more information, visit the company's website at www.ge.com
Role Summary/Purpose
Support the Clinical Affairs Project Mgr (CAPM) in planning/coordination activities around the conduct of clinical trials; incl. all operational aspects of a clinical project. Supports the team to achieve quality results in a cost-effective & timely manner. Supports CAPM & cross-functional study team in the successful execution of assigned clinical trials from protocol concept through to clinical study report, in compliance with international GCP guidelines/regulations & GEHC policies/procedures
Essential Responsibilities
• Collaborate closely with CAPM's and Clinical Research Associates, cross-functional study teams and all Research partners, internal and external to GEHC
• Support the implementation and management of clinical research studies through file management and clinical project document control.
• Assist the clinical project teams in project related activities, such as:
• Review and track site-specific, clinical trial documentation including,
• keep and maintenance of the Clinical History Files (CHF)
• Upload and maintain study documents in internal databases
• Track study metrics and study timelines
• Coordinate and participate in study team meetings and draft meeting minutes and agendas
• Support finance payment process for clinical research
• Provide administrative support to the Clinical Affairs team as required
• Assist in the planning and preparation for investigator meetings and monitoring visits
• Coordinate travel arrangements, when necessary
• Some travel may be required
Qualifications/Requirements
• Bachaler degree (or internationally recognized equivalent.)
• Minimum of one year's administrative support experience.
• Demonstrated ability to work well independently & in a team setting.
• Strong problem solving, influencing and negotiation skills.
• Excellent verbal and written communication skills with the ability to communicate business issues in English in an easy to understand manner.
• Demonstrated ability to develop and maintain positive and productive working relationships with internal and external stakeholders.
• Proficient in Microsoft Office (Outlook, Word, Excel, Project, PowerPoint)
Desired Characteristics
• Bachelor's degree (or internationally recognized equivalent) in a life sciences related field or R.N.
• Advanced capabilities Microsoft Office (Outlook, Word, Excel, Project, PowerPoint).
• Clinical Research experience such as: study site research coordination or management; sponsor-level clinical research project team experience. Other experience may include investigator qualifications; study monitoring; Clinical QA Auditing and/or Clinical Data Management within the pharmaceutical or medical device industry. (Medical Device research preferred.)
• Project management experience including the ability to prioritize, plan & evaluate deliverables; is well organized and structured, strong attention to detail.
• Experience working across cultures/countries/sites.
• Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment.
公司介绍
联系方式
- Email:Lei.zhu@ge.com