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From the employer's careers site First seen 26 Oct 2026

Medical Information Manager

GSK senior full-time

The employer hasn't listed a salary.

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Description

A Medical Information Manager plays a critical role in ensuring that MI content is scientifically balanced, evidence-based, up to date and meets the scientific needs of customers to help inform clinical care and formulary access decisions and other strategies which can have significant impact on the appropriate use of GSK products.

Key Responsibilities:

  • Creating, updating and reviewing medical information content on GSK products to ensure complex scientific content is summarized in a concise, simple and balanced manner utilizing the highest level of evidence and critically evaluating the data and literature.
  • Primary Medical sign off for the review of promotional materials to ensure compliance with relevant SOPs and written standards.
  • Planning and maintaining a robust and up to date MI database including launch readiness plans that meets the scientific needs of customers through partnership with key stakeholders.
  • Maintain deep scientific and therapeutic expertise on assigned products and understanding of MI requirements across geographies.
  • Creating and updating US medical information payer content by collaborating and building a strong relationship with our partners.
  • Collaborating with internal Medical Affairs to create/update/localise topic specific presentations to be used reactively or proactively with HCPs to share new information regarding a GSK product/disease state or help fulfil knowledge gaps.
  • Contributing actively in a Therapeutic Area cross-functional team to discuss strategic priorities of GSK product(s).
  • Impart product and disease training to the relevant US medical and/or sales teams and Global MI/ MI Contact Center staff as needed.
  • Actively participating in Medical Information Workstreams to develop best practices, ways of working and continuous development and improvement for Medical Information deliverables.

Basic Qualifications:

  • Pharm.D, PhD or equivalent.
  • 2 or more years post-graduate clinical/pharmaceutical industry experience.
  • 2 or more years of experience clinical literature evaluation.
  • Ability to travel up to 15%.

Preferred Qualifications:

  • Scientific knowledge and experience in Vaccines is a plus.
  • 2+ years of experience with reviewing US promotional materials.
  • 2 plus years of experience developing scientific or medical information material for HCPs, Payers, Patients, Public Health Authorities or Integrated Delivery Network (IDN) customers.
  • 3-5 years of extensive and relevant scientific experience in a pharmaceutical, managed care, or Health System setting.
  • Experience working with global teams.
  • Experience influencing internal and external stakeholders on priorities and needs to fill scientific data gaps or needs of HCPs, Payers, Patients, IDN, Public Health Authorities or Government Customer.
  • Strong communication skills.
  • Ability to work independently and manage/prioritize multiple projects simultaneously.
  • Ability to summarize complex scientific literature, real-world evidence, CER, and other observational research studies for scientific evaluation needs by various 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.

Benefits: GSK offers a comprehensive benefits program to US employees.

Skills

Required

Nice to have

  • Vaccines
  • US promotional materials
  • scientific writing
  • global teams
  • influencing stakeholders
  • communication skills
  • project management
  • scientific evaluation
  • conflict resolution
Apply on GSK