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MSD
MSD
Sponsor pentru viza H1BAsistență medicalăBiotehnologieLogistică

MSD este o companie biofarmaceutică globală care dezvoltă medicamente și vaccinuri pentru provocări majore din domeniul sănătății, inclusiv cancerul, bolile infecțioase, afecțiunile cardiovasculare și metabolice, precum și îngrijirea axată pe prevenție. Cunoscută sub numele Merck & Co., Inc. în Statele Unite, Canada și Puerto Rico, MSD îmbină cercetarea științifică cu expertiza în dezvoltare și comercializare pentru a oferi soluții de îngrijire a sănătății oamenilor și animalelor.

Activitatea sa acoperă domeniile Sănătății Umane, Sănătății Animalelor și Cercetării și Dezvoltării, creând oportunități pentru profesioniști din echipe științifice, clinice, comerciale, operaționale și corporative. Prin activitățile desfășurate în regiuni din întreaga lume, carierele la MSD reflectă accentul pus pe cercetare, colaborare, incluziune și progres responsabil în domeniul sănătății globale.

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Director, Global Scientific and Value Content – Payor

Lead global scientific and value content strategy for payor medical affairs at MSD. Oversee scientific planning, payer-focused content, cross-functional programs, analysis, and team development.

USStatele Unite ale AmericiiNJNew JerseyPAPennsylvania
190.800 $ – 300.300 $ / an
HibridNormă întreagăLiderLimbă Obligatorie: englezăManager de marketing de conținut

Descriere

  • Define and guide V&I Plans and the Scientific Platform
  • Develop, prioritize, and deliver annual GSVC product plans aligned with V&I Plans and the Scientific Platform
  • Engage stakeholders and integrate medical insights into product planning
  • Direct the development, review, approval, and communication of GSVC content
  • Create or delegate medical information letters, FAQs, disease and product slide decks, congress booth materials, and digital medical content
  • Evaluate materials for scientific accuracy, relevance, appropriate literature, internal information, and company standards
  • Coordinate stakeholder input for content development, review, and approval, including CRT prioritization and reviewed-content management for the Payor team
  • Communicate approved materials to Medical Information and Global Medical and Scientific Affairs stakeholders
  • Develop globally reusable materials with Outcomes Research and address payer-landscape requirements
  • Act as a subject-matter expert and lead complex product projects and initiatives
  • Mentor and support GSVC P3/P4 staff and newly hired V&I GMVC team members
  • Lead internal training on GSVC disease and product content
  • Collaborate globally with Publications, Medical Directors, Payor and Health System Medical Affairs, Compliance, PDT, Outcomes Research, MSLs, and other stakeholders
  • Direct complex cross-functional initiatives and departmental process improvements
  • Write and maintain SOPs and lead organizational or cross-organizational initiatives
  • Coordinate coverage and contribute as a medical writer for Global Input Meetings
  • Provide strategic direction on complex issues, escalations, regulatory and compliance matters, and team objectives
  • Perform quantitative and qualitative analyses and communicate findings
  • Lead onboarding and training for core functions
  • Promote change, innovation, and cross-functional collaboration

Cerințe

  • MD, PharmD, or PhD with at least five years of relevant Medical Affairs experience; or MSN, BS in Pharmacy, or MS in Life Sciences with at least 10 years of relevant Medical Affairs experience; or BS in Nursing or Life Sciences with at least 15 years of relevant Medical Affairs experience
  • Deep knowledge of healthcare systems and payer processes and environments
  • Relevant pharmaceutical-industry experience in Medical Affairs or Outcomes Research
  • Demonstrated leadership through initiatives, mentoring, process improvement, and innovation
  • Excellent scientific writing and verbal communication skills
  • Ability to build networks, set priorities, and collaborate across functions
  • Strong organizational and prioritization abilities
  • Effective multitasking and problem-solving skills
  • Advanced degree preferred
  • Experience with global health systems and expertise in payer organizations
  • Experience leading multiple global or regional Medical or Scientific Affairs Plans
  • Experience with promotional review or medical and legal review processes
  • Ability to create or present scientific content for scientific exchange with external customers
  • Ability to negotiate with cross-functional teams
  • Experience working across geographies with varying regulatory and compliance requirements
  • Broad knowledge spanning multiple related therapeutic areas
  • Strong analytical capability with the ability to turn strategy into action plans
  • Established mentoring experience
  • Ability to work effectively in a complex, global, team-based organization
  • Visa sponsorship is not available
  • Must reside in the United States or Puerto Rico

Beneficii

  • Annual bonus
  • Long-term incentive, where applicable
  • Medical, dental, and vision coverage
  • Additional insurance benefits for employees and families
  • Retirement benefits, including a 401(k) plan
  • Paid holidays
  • Vacation leave
  • Compassionate leave
  • Sick leave
  • Hybrid work arrangement
  • 10% travel

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