Senior Manager, Payer Value & Outcomes

🔥 18 minutes ago

🏄 California, Illinois, +2 more states – Remote

🏄 California – Remote 🌽 Illinois – Remote 🍂 Massachusetts – Remote 🔔 Pennsylvania – Remote

💵 $152k - $228k / year

⏰ Full Time

🟠 Senior

👔 Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Jazz Pharmaceuticals

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2003

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

Healthcare • Manufacturing • Biotechnology

Jazz Pharmaceuticals is a biopharmaceutical company dedicated to developing innovative medicines that address serious unmet medical needs. With a strong commitment to research and development, Jazz focuses on creating life-changing therapies, emphasizing the importance of collaboration, diversity, and employee engagement in its operations. The company prides itself on transforming patients' lives through its meaningful product offerings and a culture that fosters enthusiasm and flexibility.

📋 Description

• 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

• 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

• 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

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