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Assoc Director, Medical Information

Gilead Sciences
Foster City, United Statesfull_timeVerifiedPosted 11 May 2026
💰 $253,220/yr($177,905/yr$253,220/yr)

About the role

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
 

At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.

We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. 

As a Assoc Director, Medical Information, at Gilead you will ...
 

Responsibilities 

  • Responds to unsolicited medical requests regarding Gilead products from HCPs, members of the public, and internal Gilead colleagues. Responses are provided in a timely manner using approved scientific response documents, up-to-date literature support, and other resources 

  • Uses scientific and MI expertise to drive strategic initiatives and empower Gilead partners, HCPs, and patients to enable timely, informed decisions and improved patient outcomes 

  • Performs appropriate medical review for promotional and/or medical materials 

  • Prepares global scientific resources in collaboration with local affiliate teams  

  • Identifies, reports and records adverse events and product complaints in a timely manner in accordance with SOP. 

  • Contributes to development of GMI strategy and represents GMI cross-functionally 

  • May lead department-wide and/or global projects, initiatives, and product launches
     

Routine responsibilities may include the following:

  • Develop and maintain a deep knowledge of product, disease state and competitor landscape for assigned therapeutic area 

  • Respond to unsolicited requests for medical and scientific information regarding Gilead products and documents in the request handling system  

  • Research and collaborate with cross-functional colleagues to address complex requests.  

  • Create, update, and participate in review, quality check and approval of MI response documents  

  • Collaborate with affiliate MI and relevant internal partners who may include medical affairs, development, regulatory, global patient safety and operations, commercial, to manage global response topics and content 

  • Prepare and approve data on file to support response documents and complex requests 

  • Maintain document repository with routine review of approved documents for new data from regulatory updates, scientific conferences, up-to-date literature searches, proactive literature surveillance, or newly published materials 

  • Understand the needs and preferences of internal and external partners and customers 

  • Review and provide analysis of MI databases for trends, customer insights and data gaps to guide content development and prepare customer interaction reports to share with internal stakeholders 

  • Participate and support MI booths at scientific congresses  

  • Serve as liaison for department specific training for new staff members, cross-functional  colleagues and vendors, as required 

  • Contribute to departmental strategic initiatives by supporting key activities within the TA, including product launches, labeling updates, patient engagement etc. 

  • Execute and drive global MI initiatives and actions in a timely way to advance the provision of MI to improve patient care 

  • Identify, report and record adverse events and product complaints in a timely manner in accordance with SOP 

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Company

Gilead Sciences

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