青岛招聘

In this role, you have the opportunity to

- Do 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
- 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，致力于在从健康的生活方式及疾病的预防、到诊断、治疗和家庭护理的整个健康关护全程，提高人们的健康水平，并改善医疗效果。飞利浦将凭借先进技术、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。公司目前在诊断影像、图像引导治疗、病人监护、健康信息化以及消费者健康和家庭护理领域处于领先地位。

公司总部位于荷兰，2017年健康科技业务的销售额达178亿欧元，在全球拥有大约74,000名员工，销售和服务遍布世界100多个国家。

中国作为飞利浦全球第二大市场及像荷兰一样的“本土市场”，拥有庞大的业务规模。立足本土创新，成立飞利浦中国研究院、飞利浦医疗影像中心，面向全球提供技术支持、解决方案和优质产品。