In this role, you have the opportunity to
assess and create tailored clinical evidence packages to help bring our products successfully to the Chinese market. You will be part of a cross-functional team and act as the clinical liaison between key stakeholders in China and the business unit.
You are responsible for
As Clinical Analyst you provide the China project team with clinical data available in the medical scientific literature and expertise to weigh the evidence as part of the evidence package on the safety and performance of our medical devices. In this role you will closely collaborate with the clinical team in China. You will ensure that this data is delivered on time to enable first time right submissions.
Define clinical planning and strategy to support regulatory submissions in China
Support the China project team by providing analysis of clinical data, post-market safety data and reviews of medical scientific literature
Compile the clinical evidence package to support regulatory submissions in China
Keep up to date and assess changes in the relevant regulations and guidelines issued by the Chinese National Medical Products Administration (NMPA) on clinical evaluation of medical devices.
You are a part of
You will be part of the Clinical Science team within the Innovation and Clinical Science Department of our Image Guided Therapy Systems Business within Philips. This Business Unit is responsible for marketing, development and manufacturing of X-ray systems. Customers are interventional specialists operating in a wide variety of hospitals across the globe. The team you will be working in is a high-performance, culturally diverse team, working in a dynamic environment & driving change in a large matrix organization. The team is approx. 15 persons working in the areas of Clinical and Economical Evidence generation.
To succeed in this role, you should have the following skills and experience
MSc or PhD degree with an understanding of research methodologies & clinical study design according to good clinical practices
basic understanding of biostatistics, plus experience as a medical/scientific writer, or equivalent
strong analytical skills, a clear and concise writing style and regulatory process knowledge
Ability to work independently and as a member of the team
Experience in supporting medical device registrations in China is a strong plus
In return, we offer you
This fast-paced position will quickly give you the chance to push your career and aspirations forward within a top global healthcare company. Prove how well you can use your communication and organizational skills to achieve the project goals, and we will reward you with an attractive compensation package and the chance to stretch yourself further. Show us your energy, your creativity and your sound professional judgement, and we will match these with educational and other opportunities within a dynamic, international setting.
25 Days of leave and the possibility to purchase up to 20 extra days off annually
A variable bonus based on both Philips results and personal performance
Extensive set of tools to drive your career, such as a personal development budget, free training and coaching
Solid company pension scheme and attractive collective health insurance package
Opportunity to buy Philips shares and products with discount
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 .