Clinical Affairs Director

Philips

. Drive succession planning, talent management, and innovative evidence-generation strategies supporting business growth .

Posted 9/22/2026full-timeUnited StatesLead💰 $171,000 - $306,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical development strategy, regulatory compliance, and evidence generation within the medical device and biotech industries. Proven ability to lead cross-functional teams and engage with key opinion leaders to drive product success and market access.

Highest-signal resume keywords

Clinical Development StrategyRegulatory ComplianceEvidence GenerationPeople LeadershipMedical Device Industry Standards

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical OperationsData CollectionData AnalysisStudy DesignRegulatory AcceptabilityEvidence-Based StrategiesProduct DevelopmentLifecycle ManagementMarket AccessReimbursement

Soft Skills

Excellent CommunicationInfluencing StakeholdersCross-Functional Collaboration

Industry Keywords

Medical DevicesBiotechPharmaceuticalsISO StandardsIEC StandardsKOL EngagementReal-World EvidenceEthical StandardsGovernance PracticesHealthcare Organizations

About the role

Key responsibilities & impact

Drive succession planning, talent management, and innovative evidence-generation strategies supporting business growth
Lead translation of clinical and medical research insights into evidence-based product, regulatory, and business strategies
Integrate scientific evidence into product development, lifecycle management, and commercialization
Direct cross-functional collaboration among Clinical Affairs, R&D, Regulatory Affairs, Medical Affairs, Marketing, and external stakeholders
Balance scientific rigor, regulatory requirements, and business priorities in cross-functional decision-making
Build and maintain relationships with clinicians, KOLs, regulatory agencies, professional societies, and healthcare organizations
Use stakeholder insights to inform clinical strategy, evidence generation, and product adoption
Oversee real-world evidence strategies, including data collection, analysis, and interpretation
Establish governance practices supporting data privacy, ethical standards, and regulatory compliance
Lead clinical studies using real-world data and evidence-generation programs
Ensure robust study design, scientific validity, and regulatory acceptability
Generate evidence supporting patient outcomes, market access, reimbursement, and long-term product success
Shape regulatory policy and industry standards
Position the organization as a leader in evidence-based decision-making

Requirements

What you’ll need

10+ years of experience in medical devices, biotech, and pharmaceutical industries, working directly for a sponsor
People leadership experience
Experience with radiology-related devices or similar
Strong knowledge of relevant medical device industry standards and regulations, including ISO and IEC
Strong experience in clinical development strategy
Experience in clinical operations
Experience with Medical Affairs KOL engagement
Bachelor’s/Master’s Degree in Science or equivalent
Advanced degree preferred
Ability to perform minimum physical, cognitive, and environmental job requirements with or without accommodation
Excellent communication and ability to influence cross-functional stakeholders using clinical expertise and knowledge of medical device regulations and research standards
Willingness and ability to travel up to 25%
US work authorization required; candidates requiring current or future visa sponsorship will not be considered

Benefits

Comp & perks

Annual incentive bonus may be offered
Sales commission may be offered
Long-term incentives may be offered
Generous PTO
401k with up to 7% match
HSA with company contribution
Stock purchase plan
Education reimbursement
Comprehensive Philips Total Rewards benefits program