Philips Clinical Development Scientist 

United States, California, San Diego 

973784816

Clinical Development Scientist

Clinical Development Scientist (San Diego, CA)

The Clinical Development Scientist will be responsible for supporting evidence-generation processes for New Product Introduction (NPI) and Life Cycle Management (LCM) initiatives, working under direct supervision of the Clinical Development Manager, Clinical Affairs. The role performs literature searches, analyzes clinical data, and contributes to the development of robust clinical plans aligned with project objectives. The role collaborates actively with cross-functional teams, handles clinical studies, and assists in authoring Clinical Evaluation Reports (CERs) and regulatory submissions. The role troubleshoots data-related issues, understands global clinical evidence requirements, and presents findings to stakeholders.

Your role:

• Perform comprehensive literature searches and in-depth reviews to support evidence-generation processes for both New Product Introduction (NPI) and Life Cycle Management (LCM) initiatives, working under direct supervision.
• Analyze clinical data meticulously and contribute substantively to the development of robust clinical plans that align with project objectives.
• Collaborate actively with cross-functional teams to develop comprehensive NPI clinical deliverables, including meticulously crafted validation plans and clinically sound evaluation plans.
• Monitor and perform day-to-day management of assigned clinical studies, ensuring seamless coordination with Clinical Operations (Clin Ops) and Biostatistics & Data Management (BS&DM) teams.
• Document meticulously and provides valuable assistance in crafting Clinical Evaluation Reports (CERs), Clinical Study Reports (CSRs), and clinical sections of regulatory submissions.
• Troubleshoot issues related to clinical data collection, analysis, and reporting, ensuring the integrity and accuracy of study outcomes.
• Develop a profound understanding of global clinical evidence requirements and regulatory pathways to inform strategic decision-making and compliance efforts.
• Presents findings eloquently and provides cogent recommendations from literature reviews and data analyses to internal stakeholders, fostering informed decision-making processes.
• Acquire and apply extensive domain knowledge in technology and/or therapeutic areas, leveraging it effectively to support and enhance clinical development activities.
• Interact closely with colleagues to determine and implement optimal approaches for evidence generation and clinical study design, fostering a culture of innovation and excellence.

You are the Right Fit:

• Bachelor’sDegree in Life Sciences or Healthcare Related Fields with at least 4 years of experience in the medical device industry. MS Degree with at least 2 years of related experience.
• Awareness of importance of IP generation and protection / in identifying and initiating new methods of diagnosis, treatment and/or care
• Experience with clinical data analysis.
• Understanding of the needs and operations related to a clinical study.
• Familiarity with the following therapeutic areas: Pacemakers, Defibrillators, Cardiac Resynchronization Therapy, Electrophysiology, Holter Monitoring, Ambulatory ECG preferred.

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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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion .

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consider candidates who require sponsorship for a work-authorized visa, now or in the future.

be provided for this position. For this position, you must reside inwithin commuting distance to San Diego, CA