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Gilead Sciences

Associate Director, Medical Affairs

Gilead Sciences

. Support a portfolio of early lifecycle and pipeline programs across multiple disease areas .

Posted 9/29/2026full-timeUnited StatesSenior💰 $177,905 - $253,220 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Scientific Communications and Publications within the biopharmaceutical industry, with a strong focus on developing evidence-based narratives and managing complex communication deliverables. Proficient in navigating regulatory environments and ensuring compliance with publication standards and Medical Affairs content development.

Highest-signal resume keywords
Scientific CommunicationsPublications ManagementMedical Affairs Content DevelopmentRegulatory ComplianceStakeholder Engagement

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Scientific WritingEditingPresentation SkillsPublication PlanningEvidence EvaluationContent DevelopmentProject ManagementData SynthesisCommunication StrategyMedical Review Processes
Soft Skills
Influencing StakeholdersPlanningPrioritizationDecision-MakingCollaboration
Tools & Technologies
Medical Review SystemsContent Management SystemsPublication Management Tools
Industry Keywords
Biopharmaceutical IndustryClinical EvidenceICMJE StandardsGood Publication PracticeCell TherapyOncologyHematologyMultidisciplinary TeamsGlobal Medical AffairsComplex Therapeutic Areas

About the role

Key responsibilities & impact
  • Support a portfolio of early lifecycle and pipeline programs across multiple disease areas
  • Lead defined scientific communication workstreams spanning publication strategy and execution, scientific narrative development, evidence translation, congress activity and Medical Affairs content
  • Develop and maintain evidence-based scientific narratives as clinical evidence, the external scientific landscape and program priorities evolve
  • Develop and review field medical resources, FAQs, congress materials and other scientific communication assets
  • Adapt scientific communications to audiences, formats and channels while maintaining accuracy, balance and consistency
  • Partner with field medical teams and stakeholders to understand scientific exchange needs and translate complex evidence into practical resources
  • Monitor and synthesize external scientific, clinical and treatment landscape developments
  • Translate scientific and stakeholder insights into communication strategy, content development and evidence dissemination recommendations
  • Support congress strategy, planning and execution
  • Ensure alignment across publications, scientific narratives, congress activity and Medical Affairs content
  • Ensure communications comply with company policies, governance processes, Medical, Legal and Regulatory review requirements and external standards
  • Translate program objectives, Medical Affairs priorities, scientific evidence and landscape developments into publication priorities and executable plans
  • Guide development, scientific review and delivery of peer-reviewed manuscripts, congress abstracts, posters, oral presentations and related deliverables with agency partners
  • Partner with subject-matter experts, external authors, investigators, alliance partners and stakeholders on publication tactics
  • Represent Publications in cross-functional forums and provide updates, recommendations and escalation of material issues
  • Contribute to Global Publication Planning Team discussions and maintain publication plan documentation
  • Oversee publication vendors, medical writing partners and external resources, including scope, timelines, scientific quality and performance

Requirements

What you’ll need
  • BA/BS and 10 years relevant experience, MA/MS and 8 years relevant experience, or PhD and 2 years relevant experience
  • Relevant experience in Scientific Communications, Publications, Medical Affairs or a closely related discipline within the biopharmaceutical industry, academia or a medical communications environment
  • Demonstrated experience independently leading complex scientific communication deliverables or workstreams in a regulated environment
  • Demonstrated ability to critically evaluate scientific, clinical, translational and/or real-world evidence and communicate its implications accurately and clearly
  • Demonstrated experience developing and reviewing scientific publications and Medical Affairs content
  • Experience working effectively in multidisciplinary and matrix teams
  • Advanced scientific or clinical degree, or an equivalent combination of relevant scientific education and substantial professional experience
  • Experience contributing to integrated scientific communication and/or publication strategies
  • Experience working across multiple assets, programs, disease areas or lifecycle stages
  • Strong knowledge of publication standards and scientific communication best practices, including ICMJE and Good Publication Practice
  • Knowledge of Medical Affairs content development, governance and review processes, including Medical, Legal and Regulatory review
  • Excellent scientific writing, editing, presentation and verbal communication skills
  • Demonstrated ability to influence senior, cross-functional and external stakeholders without direct authority
  • Strong planning, prioritization and decision-making skills, with the ability to work independently, manage competing priorities and operate effectively in ambiguity
  • Experience managing external vendors, agencies, budgets or complex external partnerships
  • Experience working in global, regional or multi-country Medical Affairs environments
  • Experience in cell therapy, oncology, hematology or another complex specialty therapeutic area
  • Experience with publication planning, content management or medical review systems

Benefits

Comp & perks
  • Discretionary annual bonus eligibility
  • Discretionary stock-based long-term incentives eligibility may vary based on role
  • Paid time off
  • Company-sponsored medical insurance
  • Company-sponsored dental insurance
  • Company-sponsored vision insurance
  • Company-sponsored life insurance
  • Equal employment opportunity and reasonable accommodation support