Philips Senior Clinical Solutions Manager 

United States, California, San Diego 

191272451

The Senior Clinical Solutions Manager will play a critical role within Philips Ambulatory Monitoring & Diagnostics (AM&D) Chief Medical Office, responsible for implementing strategic medical plans aligned with business objectives, considering market dynamics and regulatory requirements.

Your role:

• Cultivates professional relationships with medical and scientific experts, ensuring effective communication of pertinent literature and complex ideas to internal and external audiences.
• Develops and delivers clinical information in response to the needs of internal/external customers, leveraging key partnerships to enhance communication efficacy.
• Utilizes advanced analytical skills to address high complexity issues efficiently and apply conceptual thinking to develop innovative solutions/strategies.
• Contributes to the development and dissemination of clinical materials in response to the needs of internal/external customers, ensuring the delivery of accurate and timely information.
• Engages in collaborative efforts within Chief Medical Office (CMO) function groups to ensure the successful implementation of safety and quality initiatives, fostering a culture of excellence.
• Partners with cross-functional product development teams across the business domestically and internationally, including Marketing, Product, R&D, Quality, Regulatory, Operations and Clinical Affairs, to drive coordinated efforts towards product advancement and compliance.
• Contributes to the implementation of global publication plans, assisting with drafting manuscripts, abstracts, and presentations in collaboration with cross-functional teams.

You're the right fit if:

• You’ve acquired a minimum of 7+ years’ combined experience in Clinical Research and/or Medical/Clinical Affairs within an FDA regulated medical device industry, and direct patient care activities, with a focus on cardiac monitoring products like wearable/Holter monitors, event recorders, or implantable loop recorders.
• You demonstrate knowledge of ECG tracing interpretation and arrythmia mechanisms.
• You’re able to effectively manage, communicate, influence and cultivate relationships with Internal/External Stakeholders, KOL’s, HCPs, and scientific professionals at all levels.
• You have proven experience working with Quality and Regulatory (Q&R) teams to assess safety and performance across the product portfolio, contributing to the assurance of product efficacy and regulatory compliance
• You have a minimum of a Master’s Degree in a Medical Science discipline (Required); MD (Doctor of Medicine), PhD desired.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality. healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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Philips Transparency Details:

• The pay range for this position in San Diego, CA is $144,000 to $231,000.

• US work authorization is a precondition of employment.
  The company will NOT consider candidates who require sponsorship for a work-authorized visa, now or in the future.
• Company relocation benefits will not be provided for this position.
  For this position, you must reside in or within commuting distance to San Diego, CA
  .
• May require travel up to 10%.