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Medical Director

GE通用电气(中国)医疗集团 2016-12-11发布 2017-01-23截止
  • 学历要求: 本科
  • 英语要求: 熟练
  • 年龄要求: 不限
  • 专业要求: 不限
  • 工作年限: 五年以上
  • 月薪范围: 面议
  • 职位性质: 全职
  • 工作地点: 上海市
  • 职称要求: 不限
  • 招聘人数: 若干

职位描述

Essential Responsibilities
-To be responsible that project activities and milestones are planned, agreed and achieved
according to the overall clinical development plan, to include pre and post marketing activities.
-To be responsible for the timely and accurate completion of project documentation such as
protocols, amendments, case report forms and study reports
-Verifies scientific accuracy of safety and efficacy summaries for regulatory/ commercial purposes
and assists with the clinical sections of regulatory dossiers and or product specific scientific
discussion, depending on pre or post-marketing activities
-Responsibility for developing and maintaining the overall medical strategy of the assigned
product(s), for validating this strategy with appropriate internal or external experts and for agreeing
the strategy with the appropriate internal business stakeholders.
-To provide clinical leadership in cross+functional project and product teams
-Working with the Quality Assurance and Regulatory Affairs teams to establish and maintain
strong risk assessment and management processes for decision-making
-Input into Risk Management reviews as it relates to patient safety, the performance of risk
assessment in the design of new products, and the interpretation of patient safety and risk in the
post-market environment.
-Collaborating with multiple functions to ensure patient safety, minimize risk, select products for
development with the greatest clinical unmet needs, work with teams and outside experts to
design robust products and to support clinical research strategies for regulatory approval,
reimbursement and adoption
Quality Specific Goals:
1.Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality
Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job
type/position
2.Complete all planned Quality & Compliance training within the defined deadlines
3.Identify and report any quality or compliance concerns and take immediate corrective action as
required
4.Drive compliance/closure of Regulatory and Quality requirements before approving Design
Control Functional Design Reviews and New Product Introduction program milestones
5.Identify continuous improvement activities by initiating the implementation of process and
product quality improvement initiatives
Qualifications/Requirements
1.Medical Degree or equivalent with relevant Clinical experience
2.Experience in GCP Clinical trials
3.Post –Graduate training or Medical experience in Radiology is desirable
4.Good written and oral communication skills,
5.Ability to work independently and systematically
6.Good interpersonal skills to build good working relationships both internally and externally
7.Experience managing complex projects and/or across global regions desirable
8.A minimum of 5 years Medical Diagnostic (Cardiology) or Pharmaceutical industry experience
9.Excellent team player with global mindset
10.Prior experience working with Microsoft office products (Word, Excel, PowerPoint)
11.Must be willing to travel as required
Desired Characteristics
1.Excellent skills in written and verbal presentation
2.Board-certification in Cardiology or Nuclear Medicine, with industry experience

联系人: Zhang Fan

地    址:北京市经济技术开发区永昌北路1号

GE 医疗集团隶属于GE(通用电气)公司,为全世界提供开创医疗护理新时代的革新性医疗技术和服务。GE医疗集团在医学成像、信息技术、医疗诊断、患者监护系统、药物研发、生物制药技术、卓越运营和整体运营解决方案等领域拥有广泛的专业技术,能够帮助客户以更低的成本为全世界更多的人提供更优质的服务。GE医疗集团还和医疗行业领袖加强合作,全力支持全球政策的发展,助力打造成功的、可持续的医疗体系。

GE医疗集团总部设在英国,员工分布于全球100 多个国家和地区,致力于为医疗专业人士和患者服务。

2009 年5 月,GE在全球启动“健康创想”战略。根据该战略,GE 承诺在六年内投资 ...详情

单位概况

GE通用电气(中国)医疗集团
近两周应聘简历处理率:36%
医疗设备/器械
医药企业 其他
1000~9999人
北京市经济技术开发区永昌北路1号
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