Director, HEOR – Contract

Adverum Biotechnologies

Director leading HEOR evidence generation for Adverum’s gene therapy and ophthalmology portfolio. Shaping global product strategy, lifecycle planning, and cross-functional stakeholder decisions.

Posted 8/5/2026contractRemote • California • 🇺🇸 United StatesLead💰 $75 - $130 per hourWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in Health Economics and Outcomes Research (HEOR) strategy development, with a strong focus on evidence generation, regulatory compliance, and cross-functional leadership in the pharmaceutical industry. Proven ability to navigate complex product development landscapes and engage with senior management to drive commercial success.

Highest-signal resume keywords

HEOR Strategy DevelopmentOphthalmology/Retina ExperienceGlobal Regulatory KnowledgeCross-Functional Team LeadershipClinical Development Expertise

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

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

Hard Skills

Evidence Generation StrategiesProgram Design and ExecutionPost-Marketing Product Life Cycle ManagementData Communication ExcellenceRegulatory ComplianceTherapeutic Area Portfolio PlanningClinical Research ManagementStrategic Impact CommunicationHTA and PR&A Landscape KnowledgeCreative Problem Solving

Soft Skills

Executive PresenceGoal OrientationSelf-Starter MindsetInterpersonal CommunicationLeadership in Global Teams

Certifications & Qualifications

Advanced Degree (MD, PharmD, or MS)

Industry Keywords

Pharmaceutical IndustryHealth Field TrainingComplex Governmental RegulationsClinical DevelopmentPipeline Development

About the role

Key responsibilities & impact

Lead the development and execution of evidence generation strategies across marketed and pipeline assets, indications, and geographies
Oversee the design and conduct of multiple programs and communicate findings and strategic impact to internal and external audiences
Serve as HEOR strategy lead with cross-functional brand teams
Determine global development strategy for new or marketed products and contribute to Therapeutic Area Long Range Plan and Portfolio Planning
Drive design and execution of HEOR programs supporting pipeline and on-market products while meeting ethical, scientific, regulatory, commercial, and quality requirements
Develop and execute post-marketing product life cycle and labeling strategies across the therapeutic area portfolio
Ensure scientific and communication excellence of agreed data elements
Deliver the HEOR book of work from strategy development through content pull-through
Partner with HEOR COE functions to represent a comprehensive HEOR voice in cross-functional meetings
Engage senior leaders and demonstrate executive presence in cross-functional settings

Requirements

What you’ll need

Advanced degree: MD, PharmD, or MS
Minimum of ten years of working experience with a Master’s, or seven years with a PhD; fellowship experience may be included
Professional training in a health field is a plus
Ophthalmology/Retina experience is required
Experience leading complex products and/or clinical development supporting pipeline development and on-market product support
Pharmaceutical industry experience preferred
Ability to work in uncharted territory with few established guidelines or procedures
Ability to direct compliance with complex governmental rules and regulations
Ability to develop creative and effective solutions to priority conflicts, resource constraints, and other problems across multiple programs
Extensive knowledge of the global regulatory, HTA, and PR&A landscape
Understanding of development-related functions across all phases of drug development
Proven leadership skills in a cross-functional global team environment
Ability to interact with senior management globally and act as HEOR project/group champion and spokesperson
High goal orientation, self-starter mindset, and strong desire to achieve commercial success
Ability to lead cross-functional teams and manage scientific personnel in clinical research

Benefits

Comp & perks

Hourly compensation of $75.00–$130.00 USD per hour
Compensation and benefits provided in accordance with specific state requirements
Paid sick leave accrual
Opportunity to contribute to meaningful work within gene therapy and ophthalmology care