Philips Clinical Analyst in Best, Netherlands

As Clinical Analyst, you provide the project teams 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. You will support Marketing to define strong claims to position our solutions in the market. You will ensure that this data is delivered on-time & the product submission is first time right.

Key areas of responsibility:

  • Support project teams by providing analysis of clinical data, post-market safety data, and reviews of medical scientific literature

  • Consult with Marketing, Q&R and Legal to support Claim substantiation

  • Create evidence to support Regulatory Submissions on the performance of our product based on literature

  • Responsible to deliver on-time as defined by the project team

  • Responsible for documentation of the Clinical Evaluation Procedure in compliance with the MEDDEV

  • Bridging technology strengths and weaknesses of our solutions to available (public) available medical literature

  • Maintenance of the Evidence/Documentation via Annual Planned Post Market Surveillance & Post-Market Clinical Follow-up Activities

Requirements:

  • Masters or PHD degree with an understanding of research methodologies & clinical study design according to good clinical practices (GCP)

  • Basic understanding of Biostatistics

  • Experience as a medical/scientific writer or equivalent

  • Strong analytical skills

  • A clear and concise writing style

  • Regulatory process knowledge

  • Basic understanding of Advanced Visualization Solutions

  • Ability to work independently & as a member of the team

In this role, you have the opportunity to

The Clinical Analyst ICAP is responsible for the assessment & creation of documentation to substantiate equivalence of development products & product claims, on the basis of published clinical data & post-market safety and clinical data to support Design Validation & Post-Market Maintenance. As part of a cross-functional team you collaborate with key stakeholders to help bring our products successfully to market.

You are responsible for

  • Support project teams by providing analysis of clinical data, post-market safety data, and reviews of medical scientific literature

  • Consult with Marketing, Q&R and Legal to support Claim substantiation

  • Create evidence to support Regulatory Submissions on the performance of our product based on literature

  • Responsible to deliver on-time as defined by the project team

  • Responsible for documentation of the Clinical Evaluation Procedure in compliance with the MEDDEV

  • Bridging technology strengths and weaknesses of our solutions to available (public) available medical literature

  • Maintenance of the Evidence/Documentation via Annual Planned Post Market Surveillance & Post-Market Clinical Follow-up Activities

You are a part of

An international team; you are working from the Best site.

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

  • Masters or PHD degree with an understanding of research methodologies & clinical study design according to good clinical practices (GCP)

  • Basic understanding of Biostatistics

  • Experience as a medical/scientific writer or equivalent

  • Strong analytical skills

  • A clear and concise writing style

  • Regulatory process knowledge

  • Basic understanding of Advanced Visualization Solutions

  • Ability to work independently & as a member of the team

In return, we offer you

We welcome you to a challenging, innovative environment with great opportunities for you to explore.

Our benefits are very competitive and designed around your preferences:

  • 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 (employee contribution fee 2%), and attractive collective health insurance package

  • Opportunity to buy Philips shares and products with discount

  • Healthy work-life balance

  • A relocation package will be provided and travel expenses will be covered according to Philips policies, if applicable.

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 at http://www.philips.com/b-dam/corporate/corporateblog/2016/PhilipsChronicDisease_5.jpg . 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 at http://www.philips.com/a-w/careers/healthtech/working-at-philips/working-at-philips.html on our career website, where you can read stories from our employee blog at http://www.usa.philips.com/a-w/our-people/life-at-philips.html . Once there, you can also learn about our recruitment process at http://www.philips.com/a-w/careers/healthtech.html , or find answers to some of the frequently asked questions at http://www.philips.com/a-w/careers/healthtech/faq.html .