Philips · 12 hours ago
Senior Clinical Development Scientist
San Diego, California, United States
Full-time
Onsite
Senior Level, Lead/Staff
$145K/yr - $232K/yr
10+ years expPhilips is a health technology company dedicated to improving healthcare access for everyone. As a Senior Clinical Development Scientist, you will develop and implement evidence generation strategies for complex projects in the field of coronary clinical development, collaborating with various stakeholders to ensure clinical safety and performance objectives are met.
B2BConsumer ElectronicsElectronicsLightingWellness
No H1B
U.S. Citizen Only
Responsibilities
Provide strategic input for all clinical aspects of the end-to-end coronary clinical development portfolio—from initial concept through post-market products—including study design, product development, and validation testing
Collaborate closely with both internal teams (such as project owners, regulatory, clinical study managers, statisticians, and business leaders) and external stakeholders (including clinical consultants, Key Opinion Leaders, and subject matter experts) to ensure clinical safety and performance objectives are met
Work professionally with investigators, animal test laboratories, regulatory authorities, societies, and associations to support research initiatives and regulatory compliance
Support claims, reimbursement, health economic outcomes, and market access strategies in partnership with internal teams, and take an active or leading role in the publication and dissemination of study results through scientific writing and collaboration with physicians and medical researchers
Lead or support scientific discussions with regulatory agencies and notified bodies to advance clinical and regulatory strategies, including facilitating clinical investigations, reviewing clinical evidence for marketing authorization and line extensions, and supporting sponsor regulatory inspections
Qualification
Required
10+ years of experience in a similar role in the medical device industry
Experience in representing the clinical function in cross-functional product development teams
Strong writing experience to produce quality clinical documents, including final reports
Demonstrated working knowledge of GCP, ICH guidelines, FDA regulations (21 CFR 812) and EU (ISO 14155) regulations
Deep understanding of product development and associated design controls within the operational framework of a Quality Management System for medical devices
Extensive clinical research knowledge and cross-functional understanding of clinical trial methodology and operational experience
Strong data analysis capabilities and experience with relevant software (SAS/SPSS is a plus)
Master's degree or higher in Biomedical Science, Engineering, or Health related field
Extensive experience in doing research for industry
Ability to successfully perform the minimum Physical, Cognitive and Environmental job requirements with or without accommodation
Excellent communication skills (written and verbal)
Proven ability to collaborate effectively with a variety of teams and stakeholders
Self-directed with a strong work ethic
Ability to work in a goal-oriented environment
Strong analytical thinking skills
Ability to present statistical methods and results to a variety of audiences
Benefits
Annual incentive bonus
Sales commission
Long-term incentives
Generous PTO
401k (up to 7% match)
HSA (with company contribution)
Stock purchase plan
Education reimbursement
Company
Philips
Philips is a technology company that operates in various fields, including healthcare, consumer electronics, lighting, and home appliances.
10001+ employees
Funding
Current Stage
Public CompanyTotal Funding
$4.23BKey Investors
EXOR N.V.Bill & Melinda Gates FoundationInnovative Health Initiative
2025-03-19Post Ipo Equity
2024-05-23Post Ipo Debt· $756.82M
2023-11-07Grant· $44.6M
Leadership Team
Ed Crawford
CEO Philips Lighting Company NA
Reema Poddar
President & CEO - Diagnostic & Pathway Informatics Business
Recent News
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