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Gilead Sciences

Associate Director, Multiple Myeloma

Gilead Sciences

. Lead priority workstreams and contribute to the U.S.

Posted 10/7/2026full-timeUnited StatesSenior💰 $177,905 - $253,220 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Medical Affairs strategy, evidence generation, and stakeholder engagement within the pharmaceutical industry, particularly in Multiple Myeloma and hematologic malignancies. Proven ability to translate complex clinical data into actionable medical strategies while leading cross-functional initiatives and managing projects effectively.

Highest-signal resume keywords
Medical Affairs StrategyMultiple Myeloma ExpertiseProject ManagementScientific CommunicationCross-Functional Collaboration

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
Clinical Data InterpretationEvidence GenerationPublication PlanningMedical Review ProcessesLaunch ReadinessAnalytical SkillsStakeholder Engagement PlansMatrixed Environment LeadershipOncology KnowledgeCellular Therapy Experience
Soft Skills
Excellent CommunicationInterpersonal SkillsOrganizational SkillsSolutions-Oriented MindsetBusiness Acumen
Tools & Technologies
Microsoft WordMicrosoft PowerPointMicrosoft ExcelProject Management Tools
Certifications & Qualifications
PharmDPhDMD
Industry Keywords
Pharmaceutical IndustryBiotechnologyHematologyMedical Education ProgramsAdvisory BoardsKOL EngagementCongress PlanningReal-World EvidenceClinical DevelopmentRegulatory Affairs

About the role

Key responsibilities & impact
  • Lead priority workstreams and contribute to the U.S. Multiple Myeloma Medical Affairs strategy
  • Serve as a strategic medical partner to cross-functional teams
  • Translate clinical data, treatment landscape insights, competitive intelligence, and stakeholder feedback into medical strategies and evidence-generation opportunities
  • Develop scientific communication platforms, medical content, FAQs, presentations, and field-facing resources
  • Lead or support advisory boards, expert engagement, congress initiatives, symposia, medical education programs, and stakeholder events
  • Partner with Field Medical on scientific engagement, insight generation, launch readiness, and medical priorities
  • Represent U.S. Medical Affairs in cross-functional forums, disease-area teams, governance discussions, and launch planning
  • Review and approve promotional, educational, and scientific materials for accuracy and compliance
  • Contribute to publication strategy, evidence generation, investigator-sponsored research review, and real-world evidence activities
  • Support major medical congress planning, content development, stakeholder engagement, and insight collection
  • Manage cross-functional projects, timelines, budgets, and external agency relationships
  • Improve operational effectiveness, anticipate risks, and implement practical solutions
  • Build relationships with internal stakeholders and external experts
  • Uphold scientific integrity, ethics, compliance, and patient-centricity
  • Create inclusion, develop talent, and empower teams as a people leader

Requirements

What you’ll need
  • PharmD or PhD and 2+ years of experience, or Master’s Degree and 8+ years of experience, or Bachelor’s Degree and 10+ years of experience, or High School Degree and 14+ years of experience
  • Advanced scientific or medical degree required; MD, PharmD, PhD, or equivalent advanced degree in life sciences, oncology, immunology, or a related discipline preferred
  • 5+ years of experience within the pharmaceutical or biotechnology industry, including Medical Affairs experience in hematology
  • Experience in Multiple Myeloma, hematologic malignancies, and/or cellular therapy strongly preferred
  • Strong understanding of Medical Affairs strategy, scientific exchange, evidence generation, publication planning, medical review processes and launch readiness experience
  • Knowledge of the multiple myeloma treatment landscape, clinical data interpretation, evolving standards of care, and emerging therapeutic approaches
  • Ability to translate complex clinical and scientific information into actionable medical strategies, field guidance, and stakeholder engagement plans
  • Experience leading initiatives in a matrixed environment and collaborating across Medical Affairs, Commercial, Clinical Development, Market Access, HEOR/RWE, Regulatory, and Global teams
  • Excellent communication, presentation, and interpersonal skills
  • Strong project management, organizational, and prioritization capabilities
  • Experience supporting congress planning, advisory boards, medical education programs, and KOL engagement activities
  • Collaborative, solutions-oriented self-starter with strong business acumen, sound judgment, and accountability
  • Strong analytical skills and experience translating clinical and scientific information into Medical Affairs strategies and execution plans
  • Proficiency with Microsoft Word, PowerPoint, Excel, and project management tools
  • Ability to travel domestically and internationally approximately 35%

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