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Sr. Global Director Medical Affairs - ID/HIV

USA - Pennsylvania - North Wales (Upper Gwynedd), United States

Job Description

Role Summary:

  • The Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for their assigned Therapy Areas (TA) in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commercialization teams. They collaborate with Early and Late Development our Research & Development Division functional areas, Value & Implementation Outcomes Research (VIOR), Policy, Commercial and Market Access to address opportunities in key countries. They engage with their network of scientific leaders and decision makers. This is a headquarters-based position in Our Company Research Laboratories Value & Implementation Global Medical and Scientific Affairs (Research & Development (R&D) VI GMSA).              

  • The Senior Director focused on Healthcare Implementation is a core member of the HIV GMSA team accountable for the development and execution of strategic plans to improve healthcare quality, guideline-concordant care, and implementation science research (support the application of evidence-based knowledge into policy and practice). This role will collaborate with the HIV Long-Acting Products and Pre-exposure Prophylaxis (PrEP) Value and Implementation Teams, as well as with the Healthcare Quality Improvement Center of Excellence (HQI CoE) team in Global Medical Proficiency and External Affairs (GMPEA).

Responsibilities and Primary Activities:

  • Provides strategic direction regarding the integration of implementation science principles into Value & Implementation strategic plans, including research initiatives from GMSA) and VIOR, Global Clinical Development, Biostatistics and Research Decision Sciences (BARDS) and Epidemiology. Advises cross-functional teams on the development and evaluation of implementation research proposals and initiatives, as well as dissemination of implementation science findings.

  • Conduct healthcare quality landscape assessments to determine drivers affecting high-quality care delivery (e.g., quality measures, quality improvement initiatives), identify opportunities for improvement, and collaboratively formulate evidence-based quality improvement strategies with cross-functional teams. Partners with the HQI CoE to leverage and pull through relevant training and resources developed in support of V&I planning and execution; to coordinate external engagement with professional medical societies and organizations on topics related to healthcare quality and implementation science; and for support on appropriate methods and approaches related to execution of implementation research tactics.

  • Supports execution of the annual Value & Implementation plan with medical affairs colleagues from key countries and regions.

  • Serves as an impactful member of Product Development Team sub-teams (e.g., Clinical, V & I, Commercial, Publications).

  • Contributes to the development of a single global scientific communications platform.

  • Consolidates actionable medical insights from countries and regions.

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Job Profile

Regions

North America

Countries

United States

Restrictions

Hybrid Hybrid work Hybrid work model On-site Puerto Rico residents only US and Puerto Rico residents only

Benefits/Perks

Bonus eligibility Diverse workplace Equal opportunity Equal opportunity employer Flexible work Flexible work arrangements Healthcare Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Insurance Meetings Paid holidays Retirement benefits Sick Days Vacation

Tasks
  • Collaborate with cross functional teams
  • Collaborate with partners
  • Communication
  • Communications
  • Compliance
  • Develop strategic plans
  • Engage with scientific leaders
  • Execution
  • Identify opportunities
  • Identify opportunities for improvement
  • Innovation
  • Leadership
  • Planning
  • Prioritization
  • Project management
  • Risk Management
Skills

Access Analytical Biostatistics Clinical Clinical Development Clinical Practice Commercial Commercialization Communication Communications Compliance Cross-functional Collaboration Cross-functional Teams Data Data Generation Development Education Educational meetings Epidemiology Evaluation Execution Expert input forums External Engagement Healthcare Healthcare quality Inclusion Infectious Diseases Innovation Insights Integration Interpersonal Leadership Management Manufacturing Market Access Matrix Environment Medical Medical Affairs Network Organization Outcomes Research Pharmaceutical Pharmaceutical Industry Planning Policy Prioritization Product Development Project Management Protocols Publications Quality Quality improvement R R&D Research Research decision sciences Research Initiatives Research Support Risk Management Science Scientific communication Scientific Communications Scientific Leadership Stakeholder engagement Strategic direction Strategic planning Teams Training Vaccines

Experience

10 years

Education

AS Biostatistics Business Communications Development Epidemiology Health Care Management Pharm.D Project Management Relevant experience Science

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9