Senior Manager, Payer Value & Outcomes

Jazz Pharmaceuticals

. Provide PVO-focused training, communications and resource development across the Jazz portfolio and pipeline .

Posted 11/12/2026full-timeRemote • United StatesSenior💰 $152,000 - $228,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in PVO-focused training, resource development, and medical writing within the pharmaceutical industry, ensuring compliance with regulatory guidelines and effective collaboration across teams. Proficient in managing knowledge across therapeutic areas and understanding access and reimbursement models in US managed markets.

Highest-signal resume keywords

Advanced Degree (PharmD, Ph.D, MD, NP, PA)Medical Writing ExperienceResource Approval Process ExperienceKnowledge of AMCP Dossiers and 21st Century Cures ActExperience in Managed Care and Health Policy

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical WritingResource DevelopmentPVO Training CoordinationNeeds AssessmentCompetency EvaluationValue Evidence GenerationClinical Development PlanningRegulatory ComplianceHealth Technology AssessmentPharmacoeconomic Principles

Soft Skills

Analytical SkillsWritten CommunicationVerbal CommunicationInterpersonal SkillsTeamwork Abilities

Tools & Technologies

Litmos

Industry Keywords

Biopharmaceutical IndustryUS Managed MarketsAccess and Reimbursement ModelsPopulation HealthHealth OutcomesHealth PolicyHealth EconomicsMARC Medical Material OwnerCustomer Insights AnalysisMatrixed Organization

About the role

Key responsibilities & impact

Provide PVO-focused training, communications and resource development across the Jazz portfolio and pipeline
Develop and update PVO resources across all Jazz therapeutic areas
Serve as MARC Medical Material Owner for all products and shepherd customer-facing resources through the resource approval process
Collaborate with resource vendors and internal teams
Coordinate with MedComms, GVHEOR, RWE and Market Access teams
Coordinate and execute scientific PVO-specific training
Conduct needs assessments and competency evaluations
Develop, update and coordinate PVO onboarding and Litmos training plans
Assist PVO product leads with packaging and analysis of customer insights, policy and access trends
Support development of value evidence generation and clinical development plans
Ensure compliance with applicable laws, regulations and regulatory guidelines governing commercial and scientific interactions

Requirements

What you’ll need

Advanced Degree Required (PharmD, Ph.d, MD, NP or PA)
Minimum of 5 years of post-doctoral relevant scientific work experience in a pharmaceutical industry medical writing, MedComms, medical value and access and/or related disciplines
Demonstrated proficiency in managing and maintaining knowledge in multiple therapeutic areas
In-depth knowledge of the biopharmaceutical industry and US managed markets, including various access and reimbursement models
Demonstrated familiarity with managed care, population health, health outcomes, health policy, health technology assessment, and pharmacoeconomic principles
Knowledge of AMCP Dossiers, 21st Century Cures Act, PIE Act, ICER and application of HCEI
Excellent analytical, written, and verbal communication
Medical writing and Medical Affairs resource development experience required
Resource approval process experience required
Strong personal integrity, interpersonal skills, teamwork abilities and customer focus
Ability to organize, adapt, prioritize, and work effectively in a matrixed organization and evolving/changing health care environment
Ability to travel approximately 20-30% of time
Occasional after-hours work may be required
Frequent public contact requiring professional business attire

Benefits

Comp & perks

Discretionary annual cash bonus or incentive compensation
Discretionary equity grants
Medical insurance
Dental insurance
Vision insurance
401k retirement savings plan
Flexible paid vacation
Remote work