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Gilead Sciences, Inc.

Associate Director, Medical Content Strategy & Enablement

Gilead Sciences, Inc., Foster City, California, United States, 94420

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Associate Director, Medical Content Strategy & Enablement United States - California - Foster City • Medical Affairs • Regular

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 Overview The

Medical Content Strategist

will work closely with the Senior Director, Medical Content Strategy to optimize the Medical Affairs scientific content ecosystem and execute strategies aimed to improve content planning through a data‑driven approach, leverage new content types and innovations (AI, modular content, infographics, etc.) to enable personalized scientific exchange with health care providers and patients, and streamline the review process with intelligent automation. Working in collaboration with the Medical Affairs therapeutic area teams, this person will drive the development and execution of high‑quality, engaging, and impactful medical content.

This position will support the

Oncology or Liver

therapeutic area’s and reports into the Senior Director, Medical Content Strategy as part of the Global Medical Strategy & Operations (GMSO) organization in Medical Affairs.

Key Responsibilities

Lead exploration of innovative methods and workstreams to optimize the entire scientific content ecosystem from content creation, review/approval, storage, dissemination, through insights generation that inform content strategy

In collaboration with Medical Affairs Therapeutic Area Teams, formulate comprehensive medical content plans that align with business objectives, target audience, and brand voice

Gather insights into audience needs, preferences, and behaviors to inform content creation

Determine the types of content to create, the platforms to use, and the overall structure of the content

Advise on creating or curating content, ensuring it is high‑quality, engaging, and relevant

Integrate search engine optimization (SEO) best practices into content strategy to improve visibility and reach

Plan and execute strategies for distributing content across various channels, including websites, field medical, social media, email, and other platforms

Track and analyze content performance metrics to identify what's working and what needs improvement

Work with therapeutic area authors, legal, regulatory, and other stakeholders to ensure content is created and delivered effectively

Stay abreast of country regulations and guidance that impact digital delivery of scientific information to external HCPs

Keep abreast of the latest trends and best practices in content and communication strategy

Education and Experience

Advanced scientific degree required (MD, PharmD or PhD)

Minimum 7 years experience in Medical Affairs with focus in medical communications, content strategy, and scientific engagement

Oncology or Immunology experience preferred

Must have a thorough knowledge of healthcare ecosystem, concepts, practices, regulations and Guidelines regarding drug development, clinical research, clinical use and medical writing standards

Have the ability to understand the medical concepts and terminology, knowledge of relevant therapeutic approaches and therapeutic guidelines

Strong track record of written and oral communication skills to develop and present scientific information to varied audiences and articulate messages succinctly with demonstrated experience in medical writing

Experience in digital communications is preferred

Be familiar with searching medical literature, understanding and presenting research data, the document review process, and editing and publishing requirements

Ability to work effectively in a collaborative team environment, multi‑task, adaptive to change; attentive to details

Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members

Ability to utilize a balanced approach to problems, using flexibility and persistence as appropriate

Knowledge in data analysis and biostatistics

Ability to think out of the box and seek new opportunities based on learnings from across industries

Entrepreneurial attitude is essential, e.g. challenges the status quo and takes calculated risks

Learning, agility and growth mindset

Experience with Veeva Vault PromoMats or MedDocs preferred

Additional Information TBD – Job Requisition ID: R0044805. Full‑time, Associate Director level.

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