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Medical Information Manager Specialty; Immunology

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: GSK
Full Time position
Listed on 2026-10-20
Job specializations:
  • Healthcare
    Clinical Research, Medical Science Liaison, Medical Science
Salary/Wage Range or Industry Benchmark: 90000 - 150000 USD Yearly USD 90000.00 150000.00 YEAR
Job Description & How to Apply Below
Position: Medical Information Manager Specialty, (Immunology)
About the Company

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success.

We’re uniting science, technology, and talent to get ahead of disease together. Find out more:
Our approach to R&D

Medical Information Manager

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. The Medical Information Manager has a deep understanding of the product/s and therapeutic area and serves as an influential partner to both the Medical Affairs and Commercial organizations.

A Medical Information Manager will need to possess a baseline understanding of business priorities and the scientific evidence requirements of Health Care Providers (HCPs) and understand how HCPs and population-based decision makers are using scientific evidence to inform decisions, deploy population-management programs and cost containment strategies, and control new product coverage/use.

Key Responsibilities

Creating, updating and/or 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.

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 (US Medical Affairs Leader, US Health Outcomes, Legal) so that payer and managed care organizations have the necessary resources they need to make decisions regarding GSK products.

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.

Primary Medical sign off for the review of promotional materials to ensure compliance with relevant SOPs and written standards.

Contributing actively in a Therapeutic Area cross‑functional team to discuss strategic priorities of GSK product(s), to ensure appropriate resources (e.g., medical information content) are available to meet the priorities, and to present relevant medical insights and current trends based on fulfilment of medical information content.

Impart product and disease training to the relevant US medical and/or sales teams and Global MI/ MI Contact Centre staff as needed.

Actively participating in Medical Information Work streams 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’ experience evaluating clinical literature

2 or more years’…

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