长沙招聘

In this role, you have the opportunity to

•  Broadly defined, this role is responsible for the operational execution of clinical study involving human subjects from its inception to close-out.

• Ensure robust and complete clinical plans are developed; the consistent and effective communication of clinical plans, project tracking and completion, to all internal and external stakeholders;

• Manage Contract Research Organization oversight, including staff; coordination of site visits, review reports and ensure adequate corrective action;

• Develop Clinical Evaluation Report (CER) per needs.

   

 

You are responsible for

• Ensure all the company-sponsored studies executed in compliance with GCP, related regulations, Philips harmonized clinical SOPs in terms of quality and timeframe;

• Ensures the clinical study successfully complete on time and on budget;

• Ensures the clinical study in high quality and compliant to Philips harmonized clinical SOPs and local regulation;

• Ensures the clinical study can withstand audit scrutiny by internal clinical trial audit or Regulatory entity where the risk of failure can affect product registration;

• Ensures that all internal and external collaborating staff are appropriately organized, trained and managed to execute the terms of a research project per protocol and to ensure study and data integrity in support of a broader Clinical Evidence Strategy;

• Actively interfaces with various internal and external stakeholders including clinical science teams, internal customers, Regulatory, Legal, Quality, CRO/vendor staff, Key Opinion Leaders and clinical research staff as the subject matter expert for clinical GCPs;

• Proactively identifies and independently prepares high quality clinical trial execution, project management, and reporting documentation (Protocol, Investigator Brochure and Inform Consent Form).

• Provide leadership in standardizing and optimizing clinical-related materials to Ethics Committee;

• Develop Clinical Evaluation Report (CER) per needs.

 

 

You are a part of

Great china Q&R team

 

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

• At least 4 years’ experiences in clinical research execution, including at least 1 years project management experience;

• Self-motivated individual who is able to manage multiple tasks and priorities in an efficient manner.

• Demonstrated track record of Compliance to regulations governing human clinical research.

• Demonstrated expertise of GCP and CFDA regulatory requirements for the conduct of research involving human subjects is required Effective communication and project team skills.

•  Comfortable working closely with a team taking ownership/initiative where needed, and taking/delegating task appropriately.

• Total Site Management, Budgeting, Agreement negotiation experience is required.

   

In return, we offer you

A path towards your most rewarding career. Philips is growing its marketing capability enterprise wide. Succeeding in this market-based 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.

 

• A professional but fun workplace, A healthy work-life balance environment;

• An energetic, genuine, inventive, supportive and dynamic team atmosphere;

 

 

Why should you join Philips?

Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on improving 3 billion lives a year by delivering innovative solutions across the health continuum. Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways. Learn more by watching this video.

 

To find out more about what it’s like working for Philips at a personal level, visit the Working at Philips page on our career website, where you can read stories from our employee blog. Once there, you can also learn about our recruitment process, or find answers to some of the frequently asked questions.

 

 

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。