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Associate Director, Medical Information
Gilead Sciences. Provide strategic scientific leadership for the development, delivery, and evolution of Medical Information across assigned products and therapeutic areas .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Medical Information strategy, content development, and lifecycle management while providing scientific leadership and strategic recommendations across cross-functional teams. Capable of analyzing inquiry patterns and implementing digital and AI-enabled capabilities to enhance processes and customer experience.
Highest-signal resume keywords
Medical Information StrategyContent DevelopmentDigital And AI-Enabled CapabilitiesGovernance And Risk ControlsCross-Functional Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Data AnalysisEvidence-Based RecommendationsInquiry ManagementQuality MonitoringLifecycle ManagementContent GovernanceScientific ReviewProcess ImprovementMetrics AnalysisImplementation Leadership
Soft Skills
Strategic LeadershipRelationship BuildingStakeholder AlignmentTeam EmpowermentCommunication
Industry Keywords
Medical InformationComplianceRisk AssessmentAdverse Event ReportingProduct LaunchScientific Congress ActivitiesContent DevelopmentInquiry TrendsCustomer ExperienceGlobal Alignment
About the role
Key responsibilities & impact- Provide strategic scientific leadership for the development, delivery, and evolution of Medical Information across assigned products and therapeutic areas
- Shape Medical Information strategy and influence cross-functional decision-making
- Lead high-impact initiatives, product launches, process improvements, and cross-functional projects from concept through implementation and evaluation
- Serve as a Medical Information subject matter expert on cross-functional teams
- Build relationships across functions and geographies and align stakeholders around scientifically sound solutions
- Translate customer needs, scientific developments, inquiry trends, and evidence gaps into actionable recommendations
- Lead the strategy, development, review, approval, and lifecycle management of global Medical Information response documents and scientific resources
- Collaborate with affiliate and global partners to develop globally aligned content
- Serve as a key medical reviewer for promotional, medical, and Public Affairs materials
- Guide content governance and repository stewardship
- Support scientific congress activities, vendor or contractor oversight, training, and departmental or enterprise initiatives
- Analyze inquiry patterns, customer interactions, metrics, and content gaps to generate actionable insights
- Lead or support evaluation and implementation of digital and AI-enabled capabilities
- Partner with scientific, operational, technology, legal, regulatory, privacy, and compliance stakeholders on governance and risk controls
- Improve Medical Information processes, customer experience, and global ways of working
- Lead or contribute to pilots and scaled implementation
- Create inclusion, develop talent, and empower teams
Requirements
What you’ll need- Deep knowledge of the disease state, clinical data, evidence base, and relevant competitive landscape
- Expertise in Medical Information strategy, content development, review, approval, and lifecycle management
- Ability to provide scientific expertise and strategic recommendations on cross-functional teams
- Ability to ensure scientifically accurate, high-quality, consistent, and compliant Medical Information deliverables
- Experience with digital and AI-enabled capabilities for content development, literature synthesis, inquiry management, insight identification, quality processes, or medical review
- Ability to establish governance, risk controls, quality monitoring, and accountable human oversight for technology-enabled workflows
- Ability to lead pilots and implementation, including requirements definition, risk assessment, workflow design, user adoption, quality monitoring, and impact evaluation
- Ability to ensure timely documentation of inquiries and reporting of adverse events and product complaints in accordance with applicable procedures
Benefits
Comp & perks- Discretionary annual bonus
- Discretionary stock-based long-term incentives
- Paid time off
- Company-sponsored medical insurance
- Company-sponsored dental insurance
- Company-sponsored vision insurance
- Company-sponsored life insurance