Medical Information Manager, Vaccines

GSK•Upper Providence, PA

About The Position

The Medical Information Manager ensures that medical information content is scientifically balanced, evidence-based, current, and responsive to customers’ scientific needs. This work helps inform clinical care, formulary access decisions, and other strategies affecting the appropriate use of GSK products. The role requires deep knowledge of assigned products and therapeutic areas and serves as an influential partner to Medical Affairs and Commercial organizations. The manager also needs to understand business priorities and how healthcare providers and population-based decision makers use scientific evidence to inform decisions, deploy population-management programs, manage costs, and guide product coverage and use.

Requirements

  • Pharm.D., Ph.D., or equivalent.
  • At least 2 years of post-graduate clinical or pharmaceutical industry experience.
  • At least 2 years of experience evaluating clinical literature.

Nice To Haves

  • Scientific knowledge and experience in vaccines.
  • At least 2 years of experience reviewing US promotional materials.
  • At least 2 years of experience developing scientific or medical information materials for HCPs, payers, patients, public health authorities, or IDN customers, directly or indirectly, in a global or local communications role.
  • 3–5 years of extensive and relevant scientific experience communicating and translating scientific evidence in a pharmaceutical, managed care, or health system setting.
  • Experience working with global teams.
  • Experience influencing internal and external stakeholders on priorities and needs related to scientific data gaps or the needs of HCPs, payers, patients, IDNs, public health authorities, or government customers.
  • Strong communication skills.
  • Ability to work independently and manage and prioritize multiple projects simultaneously.
  • Ability to summarize complex scientific literature, real-world evidence, CER, and other observational research studies for scientific evaluation needs across customer types.
  • Ability to operate in a highly dynamic, changing, and matrixed environment.
  • Ability to develop and maintain strong, trusted relationships with internal partners locally and globally.
  • Demonstrated customer focus, problem-solving abilities, and strong conflict-resolution skills.
  • Cross-Functional Leadership, Digital Fluency, Enterprise Thinking, High Impact Communication, Launch Excellence, and Patient Impact.

Responsibilities

  • Create, update, and review medical information content on GSK products, summarizing complex scientific content concisely and clearly, maintaining balance, and critically evaluating data and literature using the highest level of evidence.
  • Provide primary Medical sign-off for promotional-material reviews to ensure compliance with relevant SOPs and written standards.
  • Plan and maintain a robust, current medical information database, including launch-readiness plans, in partnership with key stakeholders and responsive to customer scientific needs.
  • Maintain deep scientific and therapeutic expertise for assigned products and understand medical information requirements across geographies.
  • Create and update US medical information payer content in collaboration with the US Medical Affairs Leader, US Health Outcomes, and Legal, supporting payer and managed care organization decisions about GSK products.
  • Collaborate with Medical Affairs to create, update, or localize topic-specific presentations for reactive or proactive use with HCPs, sharing new product or disease-state information and addressing knowledge gaps.
  • Contribute to Therapeutic Area cross-functional teams by discussing product strategic priorities, ensuring appropriate resources are available, and presenting relevant medical insights and trends based on medical information content fulfilment.
  • Provide product and disease training to relevant US medical or sales teams and Global MI/MI Contact Center staff as needed.
  • Participate in Medical Information workstreams to develop best practices, ways of working, and continuous improvement of medical information deliverables.
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