长沙 [切换城市] 长沙招聘长沙生物/制药/医疗器械招聘长沙临床研究员招聘

Clinical Study Manager_CIH

飞利浦(中国)投资有限公司 Philips (China) Investment Co.,Ltd.

  • 公司规模:10000人以上
  • 公司性质:外资(欧美)
  • 公司行业:多元化业务集团公司

职位信息

  • 发布日期:2020-11-03
  • 工作地点:上海-静安区
  • 招聘人数:1人
  • 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:2.5-3万/月
  • 职位类别:临床研究员  医疗器械研发

职位描述

In this role, you have the opportunity to

work with talented research team in Philips Research China, while closely collaborating with local clinical partners, global research community and business within Philips.


You are responsible for

  • Take primary responsibility to coordinate, oversee and execute the end-to-end study process for the study portfolio consisting of all study types as assigned by the Innovation Program Managers (IPMs) in the cluster-specific Study Affairs Meetings (SAMs). The study manager is a formal team member in each of the study portfolio’s research teams.
  • Serve as a full member of the SAM, specifically with regard to the strategic prioritization, study status tracking and management of his/her study portfolio.
  • Take responsibility for study-specific document submissions, amendments and closure as required by the Internal Committee for Biomedical Experiments (ICBE).
  • Liaise with Clinical Study Managers and other staff in the Clinical Operations group with regard to international and national regulatory and compliance requirements of clinical studies, including clinical investigations.
  • Provide guidance to Project Leaders, Scientists, Researchers and Research Engineers in the project teams with regard to internal and external process requirements.
  • Liaise with internal and external role players, where applicable, to contribute to the strategic continuity of project-specific objectives and priorities, including ICBE Secretaries, Clinical Research Board, study monitors, clinical site staff and third party vendors. In the case of study monitoring, it may involve responsibility for the development of the monitoring plan, training of investigators and site staff on the protocol, scheduling monitor visits and study amendments in close collaboration with the formal study monitor.
  • Manage the timely reporting of CAPAs linked to project-specific violations. This involves participation in the relevant CAPA Review Board.
  • Responsible for the reporting of Serious Adverse Events, where applicable, to internal and/or external role players in line with the applicable laws, regulations and standards.
  • Participate in internal and external project audits, where applicable.


You are a part of

Philips Research, which is the essential force of end to end innovation. Philips Research China was established in 2000. You will report to the department head. You will work with a team of passionate, professional and multi-disciplinary scientists, meantime connecting to the global Research community, relevant local/global Business and healthcare professionals.


To succeed in this role, you should have the following skills and experience

  • Bachelor degree in life sciences or related medical/scientific field. Advanced degree (Masters or PhD) in life sciences or related medical/scientific field is preferred.
  • Minimum of 5 years of research experience in a relevant medical device technology research field, including experience in conducting data studies, market research, animal studies and medical device clinical studies.
  • Experience in one or more of the following research fields is a plus, ideally in diagnostic imaging, image-guided therapy, acute care signal processing, clinical informatics and medical device research.
  • Project management skills, including strong problem solving skills, quality focus and change management skills.
  • Experience in lean and agile ways of working.
  • Demonstrated ability to work effectively in cross-functional and geographically diverse teams, including the ability to plan and facilitate face-to-face and digital meetings.
  • Excellent verbal and written communication skills, with ability to communicate to all levels of the organization
  • Currently valid Good Clinical Practice (GCP) training certificate and experience in GCP.
  • Knowledge of ISO 14155 and ISO 14971standards and requirements is a strong plus.
  • Experience in working with the following software tools: SharePoint, Windchill, ORION-ICBE is a plus.
  • Experience in the legal and commercial aspects relating to contracting in general, and contracts in the life sciences arena, in particular, is a plus.


In return, we offer you

A path towards your most rewarding career. Succeeding in this role in a complex environment will open many doors for your long term career, in other areas in Philips or otherwise. We also believe that we are at our best as a company when you are at yours as a person. Thus, we offer competitive health benefits, a flexible work schedule and access to local well-being focused activities. You will be working with a group of talented scientists who have passion to deliver meaningful innovation in imaging system.

公司介绍

荷兰皇家飞利浦公司是一家领先的健康科技公司,致力于在从健康生活方式、疾病预防、到诊断、治疗和家庭护理的整个“健康关护全程”,凭借先进的技术、丰富的临床经验和深刻的消费者洞察,不断推出整合的创新解决方案,助力健康医疗系统实现四重目标——提高大众健康水平、提高医护人员满意度、改善患者体验,并降低关护成本。飞利浦的愿景是通过有意义的创新,令世界更健康、更可持续的发展,到2030年每年改善25亿人的生活。

        飞利浦公司总部位于荷兰,2021年销售额达172亿欧元,在全球拥有大约78,000名员工,销售和服务遍布世界100多个国家。公司目前在诊断影像、图像引导治疗、病人监护、医疗信息化以及消费者健康和家庭护理领域处于领导地位。

        在飞利浦,每一个人,都至关重要。这是我们始终坚持的信念。在飞利浦,你将用数字化驱动有意义的创新,积极影响自己与数十亿人的生活,践行改善人类生活的使命。我们全心营造多元包容的工作环境,平等互助的工作氛围,让你的独特之处得到充分尊重和欣赏,鼓励你释放真我,以梦为马,不负韶华。本着 “立足中国,辐射全球” 的理念,我们通过布局广泛的业务线,为你带来广阔的平台、丰富的学习资源、多样的内部发展机会,助你成为具备全球化视野和本土深度的一专多能复合型稀缺人才。

创美好,做真我,迎蜕变。
我们深信每一个你都卓尔不凡, 更期待与志同道合的你笃行致远。

联系方式

  • Email:ruby.chen@philips.com
  • 公司地址:上海市静安区灵石路718号A1栋 (邮编:200233)
  • 电话:13774217703