Full-Time

Executive Director

Digital Communications

Posted on 9/3/2025

Gilead Sciences

Gilead Sciences

10,001+ employees

Biopharmaceutical firm developing HIV/AIDS therapies

Compensation Overview

$281k - $363.7k/yr

+ Bonus + Stock-based long-term incentives

Company Historically Provides H1B Sponsorship

San Mateo, CA, USA

In Person

US Top Secret Clearance Required

Category
Social Media (3)
, ,
Required Skills
Public Policy
SEO
Data Analysis
Requirements
  • Creating and executing a digital communications strategy, encompassing a digital vision and roadmap aligned to enterprise priorities, and ensuring digital communications integration across web, social, intranet, and emerging platforms.
  • Understanding of the public policy, ESG, stakeholder engagement, and advocacy landscape and how it contributes to overall reputation.
  • Stakeholder engagement and tailoring content for diverse audiences including employees, media, policymakers, and communities.
  • Proficiency in managing high-risk digital crisis communications and reputational issues using digital tools and real-time escalation frameworks.
  • Ability to leverage and understand analytics and metrics and how to define and interpret key digital performance indicators (KPIs), social listening tools, and campaign measurement.
  • Content and channel optimization, including understanding of SEO, user experience, mobile-first design, and content performance across platforms.
  • Familiarity with global digital governance frameworks, brand standards, and regulatory considerations in a healthcare / pharmaceutical environment.
  • Awareness of emerging digital trends including AI content tools, automation, personalization engines, and global platform usage (e.g., WeChat).
  • Experience managing and mentoring high-performing global teams, with a focus on capability-building and succession.
  • Ability to align diverse internal stakeholders and influence at all levels, including without direct authority.
  • Strong ability to modernize legacy processes, shift mindsets, and embed future-ready capabilities.
  • Skill in rapidly assessing digital threats, and other crisis response issues, and responding with clarity, consistency, and brand protection.
  • Proficiency in resource and budget management, aligning resources and spend with strategic priorities.
  • Deep understanding of how to leverage major digital platforms (LinkedIn, Twitter/X, Instagram, YouTube, TikTok, etc.) for both reach and reputation.
  • Has a ‘systems thinking mindset’ and sees the big picture, understanding the role of digital within a broader business and reputation ecosystem.
  • Action-oriented, moving with urgency and confidence, particularly in high-stakes or fast-changing environments.
  • Flexible, thriving in ambiguity and rapidly evolving digital and geopolitical environments.
  • Leads with cultural sensitivity across global markets; adapts content, tone, and platform strategy regionally.
  • Has a high level of executive presence and communicates with impact at the senior-most levels and represents the company with credibility externally.
  • Stays focused and composed through organizational change, ambiguity, and challenge.
  • Has a growth mindset and continuously learns, adapts, and inspires a culture of innovation and experimentation.
Responsibilities
  • Lead the development and execution of a global digital communications strategy within Public Affairs, aligning with enterprise brand and business goals. Define the right mix of digital channels (e.g., websites, social media, intranet, email, emerging platforms) to engage external stakeholders and employees with high-quality, impactful storytelling.
  • Oversee the full digital ecosystem for Public Affairs, including global websites, social media, digital customer engagement, and analytics, ensuring consistency, brand alignment, and innovation across platforms.
  • Proactively advise and collaborate with content teams on data-driven strategies, providing insight into which stories and formats perform best across channels. Deliver real-time counsel on how to enhance corporate reputation in response to emerging opportunities or risks.
  • Lead cross functional working groups meant to ideate, innovate and improve our content, strategies and approach across our digital channels.
  • Create a culture of accountability for digital at the organization.
  • Strengthen Gilead’s storytelling capabilities across the function, educating internal partners such as Media Relations, Corporate Social Responsibility, Employee Engagement and Environmental & Social Governance, on the unique value of each channel, while sourcing diverse content that reflects the voices and impact of our global operations.
  • Establish and lead a digital-first stakeholder engagement calendar, aligned to enterprise milestones, business priorities, and external environmental factors.
  • Launch and scale global-local digital models, including new country-level websites and social channels across Europe, Asia, and Latin America, with localized execution grounded in brand standards and innovation.
  • Create governance frameworks and training programs that empower affiliate teams while ensuring alignment with global brand and reputational standards. Set clear roles, responsibilities, and benchmarks for digital excellence.
  • Drive digital skill / capability-building across Public Affairs and various functions by improving understanding of audience insights, platform strengths, content trends, and cross-functional integration (e.g., with commercial and medical digital teams).
  • Develop and implement a digital measurement framework, in partnership with the Strategy and Operations team, defining KPIs and success metrics for all platforms and campaigns. Use data insights to optimize strategies, report progress to senior leaders, and influence broader business decisions.
  • Enhance agility around reputational issues and digital crises by establishing proactive monitoring tools, issue escalation protocols, and close coordination with Legal, Media Relations, Government Affairs and other key areas, for rapid response and brand protection.
  • Identify and pilot emerging digital technologies, such as AI, personalization engines, chatbots, and automation, to improve content creation, engagement, and operational efficiency.
  • Ensure the technical and user experience optimization of owned digital assets, including SEO, accessibility, mobile responsiveness, and intuitive navigation to maximize reach and inclusivity.
  • Lead and develop a high-performing, global digital communications team, setting a clear vision, priorities, and culture of innovation. Design team structures, processes and documentation in a way that ensures continuity of work, institutional knowledge, a culture of continuous improvement and long-term team resilience.
  • Prioritize hiring, training and mentoring to ensure the team can be proactive and achieve the needs of tomorrow, holding the team accountable for continuous learning and evolution.
  • Manage resources and budget in a cost-effective manner, while allocating resources to areas that will build long-term capability and impact.
Desired Qualifications
  • Bachelor’s Degree and 16+ years of experience, or
  • Master’s Degree and 14+ years of experience, or
  • 12+ years’ healthcare experience working in-house or in an agency in area of communications, preferred.

Gilead Sciences discovers, develops, and markets medicines to treat HIV/AIDS, liver diseases, cancer, inflammatory and respiratory diseases, and cardiovascular conditions. Its products reach patients globally after regulatory approval, sold through doctors, hospitals, and pharmacies. The company relies on a large, diverse R&D pipeline and strategic partnerships to expand its therapies and reach, including collaborations like SAP Ariba to improve sourcing. Its goal is to improve health equity by expanding access to medicines and promoting sustainable healthcare practices worldwide.

Company Size

10,001+

Company Stage

IPO

Headquarters

Foster City, California

Founded

1987

Simplify Jobs

Simplify's Take

What believers are saying

  • Lenacapavir access expansion in South Africa can model broader HIV prevention rollout.[1]
  • Hepcludex is the first U.S.-approved treatment for chronic hepatitis delta.[1]
  • Trodelvy and U.S. PrEP delivered strong recent growth, supporting near-term revenue.[1]

What critics are saying

  • Bictegravir-lenacapavir approval could fail or receive a narrow label in August 2026.
  • Trodelvy expansion depends on second-half 2026 regulatory wins for new indications.
  • Acquisition charges and added debt pressure earnings if integration misses continue.

What makes Gilead Sciences unique

  • Gilead leads in HIV, liver disease, oncology, and inflammation therapies.[1][5]
  • Its portfolio includes category-first HIV regimens and prevention medicines.[2][3]
  • The company operates globally across more than 35 countries and six continents.[1][5]

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Benefits

Paid family time off and paid parental time off

Generous 401(k) contribution matching

Comprehensive medical plans that cover both physical and mental healthcare

Global Wellbeing Reimbursement

Time Off

Global Volunteer Day

Giving Together Program

Employee Support Programs

Flexible Work Options

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
AllSci
Apr 10th, 2026
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Tempus AI expands oncology data collaboration with Gilead Sciences through AI-driven platform access. April 10, 2026 Tempus AI, Inc. (Nasdaq: TEM), a Chicago-based technology company, announced an expanded multi-year collaboration with Gilead Sciences, Inc. (Nasdaq: GILD) aimed at advancing Gilead's oncology pipeline through enterprise-wide access to Tempus's AI-driven Lens platform and multimodal real-world evidence datasets. The agreement covers multiple oncology indications; no specific drug candidates or therapeutic targets were disclosed as part of the transaction. Financial terms were not disclosed. Under the expanded arrangement, Gilead gains enterprise-wide access to the Tempus Lens platform, which integrates de-identified genomic, clinical, imaging, and outcomes data into a unified repository supported by AI-driven analytical tooling. Disclosed applications include trial design, indication selection, biomarker strategy, health outcomes analysis, and clinical real-world evidence generation. Tempus will also provide dedicated analytical services under the agreement. The collaboration represents an expansion of a pre-existing relationship in which Gilead had previously used Tempus data to inform oncology R&D initiatives, and follows on from a collaboration between Tempus and Daiichi Sankyo announced in March 2026. The collaboration is designed to operate across Gilead's oncology pipeline rather than in support of a single program. Gilead's oncology portfolio includes sacituzumab govitecan, axicabtagene ciloleucel, brexucabtagene autoleucel, and magrolimab, among other assets, though none were named as specific beneficiaries of the arrangement. The platform's stated functions - indication prioritization, patient stratification, biomarker pre-validation, and real-world evidence generation - are applicable across tumor types and development stages. Your email address will not be published. Required fields are marked *

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Gilead exercises option on Kymera's oral CDK2 degrader KT-200, triggering $45M milestone

Kymera Therapeutics will receive a $45 million milestone payment following Gilead Sciences' decision to exercise its option to exclusively licence KT-200, a first-in-class oral CDK2 molecular glue degrader development candidate. Gilead will advance the programme into IND-enabling studies, targeting an IND filing in 2027. KT-200 is expected to become the first molecular glue discovered by Kymera to enter clinical trials. The drug candidate demonstrated low-nanomolar degradation of CDK2 in preclinical testing, with robust activity in cancer cell lines and favourable safety profiles. It targets cancers driven by CCNE1 amplification, including advanced breast cancer. Under their collaboration agreement, Kymera is eligible for up to $750 million in total payments and has received $85 million to date. The company will also receive tiered royalties on net product sales.

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Gilead to acquire Tubulis for up to $5B, expanding cancer ADC capabilities.

Gilead to acquire Tubulis for up to $5B, expanding cancer ADC capabilities. April 7, 2026 Gilead Sciences has agreed to acquire German-based Tubulis for up to $5 billion, the companies said today, in a deal designed to expand the buyer's antibody-drug conjugate (ADC) capabilities with a focus on fighting cancer. Headquartered in Munich, privately held Tubulis has developed next-generation ADC candidates based on its own conjugation, linker and payload technologies intended to more selectively deliver diverse payloads to tumors deemed to be of high unmet need. The companies said Tubulis' programs and platforms have broad potential across multiple tumor types, complementing Gilead's development and commercialization expertise in oncology. "We like the strategic fit and deal terms of the Tubulis (private) acquisition," Daina M. Graybosch, PhD, senior managing director, immuno-oncology and a senior research analyst at Leerink Partners, wrote this morning in a research note. "This is more than an oncology bolt-on; we see real platform value in application of Tubulis' ADC technologies to other therapeutic areas, namely virology." Tubulis' lead pipeline candidate, TUB-040, is a sodium-dependent phosphate transport protein 2B (NaPi2b)-targeting topoisomerase-I inhibitor (TOPO1i) ADC that is now under study in the Phase Ib/II NAPISTAR1-01 trial (NCT06303505) assessing its safety, pharmacokinetics, and preliminary efficacy as a treatment for platinum-resistant ovarian cancer and non-small cell lung cancer (NSCLC). In October at the European Society for Medical Oncology (ESMO), Graybosch noted, Tubulis presented data for TUB-040 showing a confirmed 50% overall response rate (ORR) and a 60% unconfirmed ORR across dose levels and irrespective of target antigen - results that were competitive with more mature datasets from leading TOPO1i ADCs. "Though the dataset was early, and our primary outgoing question was how durability would mature, we suspect that Gilead saw durability maturing positively in their diligence," Graybosch added. "If TUB-040 proves active in NSCLC, the program could complement their Trodelvy and IO [immune-oncology] lung programs. We wonder if Gilead saw early clinical NSCLC data in their diligence and if excitement around the emerging signal drove some of Tubulis' valuation." Another Tubulis pipeline candidate, TUB-030, is a 5T4-targeting ADC that according to the companies has shown promising initial clinical data across various solid tumor types. TUB-030 is currently under study in the Phase I/IIa 5-STAR 1-01 trial (NCT06657222), a first-in-human study which aims to evaluate the safety, tolerability, pharmacokinetics, and efficacy of TUB-030 as a monotherapy in patients with advanced solid tumors. Tubulis has said it is developing TUB-030 for up to 13 undisclosed solid tumor indications. Partners since 2024. The acquisition deal follows a two-year, up-to-$465 million collaboration with Tubulis launched in December 2024. Gilead gained access to Tubulis' Tubutecan and Alco5 platforms after signing an exclusive option and license agreement to discover and develop an ADC against a solid tumor target. At the time, Gilead agreed to pay Tubulis $20 million upfront, received an option that if exercised would have given Tubulis an additional $30 million - plus up to $415 million in payments tied to achieving development and commercialization milestones, as well as mid-single to low double-digit tiered royalties on sales of marketed products resulting from the collaboration. "Today's agreement follows a two-year collaboration with Tubulis, which has given us strong conviction in their programs and research capabilities," Gilead Chairman and CEO Daniel O'Day said in a statement. "The agreement to acquire Tubulis is a significant milestone in Gilead's progress in oncology. The company brings a clinical-stage candidate that is a potential new treatment for ovarian cancer, as well as a next-generation ADC platform and a promising early pipeline." "Bringing this potential into Gilead would further expand what is already the strongest and most diverse pipeline in our company's history," O'Day declared. Investors appeared less enthusiastic about the acquisition, as shares of Gilead dipped 1.7% in early Tuesday trading to $137.80 as of 12:01 p.m. ET. Tubulis is Gilead's third announced acquisition this year. The biotech giant announced plans in March to buy Ouro Medicines for up to $2.18 billion, and in February agreed to acquire Arcellx for up to $7.8 billion - for which it agreed last week to extend its tender offer until 5 p.m. ET on April 24. Under the acquisition deal, Gilead agreed to acquire all of the outstanding equity of Tubulis for $3.15 billion in upfront cash payable at closing, and up to $1.85 billion in payments tied to milestones. The transaction is expected to close in the second quarter subject to expiration or termination of specified regulatory filings and other customary conditions. Upon closing of the deal, Tubulis will operate as a dedicated ADC research organization within Gilead, with the Munich site serving as a hub for ADC innovation, building on its integrated discovery, manufacturing, and clinical capabilities to advance next generation ADCs. Gilead said it plans to finance the transaction with a combination of cash on hand and senior unsecured notes. Gilead finished 2025 with $10.605 billion of cash, cash equivalents and marketable debt securities, up from $9.991 billion as of December 31, 2024.

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EQT Life Sciences to exit minority stake in Tubulis via sale to Gilead Sciences for up to USD 5.0 billion. Up next. Published on 07 April 2026 EQT Life Sciences plans to sell its stake in Tubulis to Gilead Sciences. * EQT Life Sciences sells stake in Tubulis to Gilead Sciences. * The transaction could be valued at up to $5 billion. * This sale marks a significant shift in EQT's investment strategy. EQT Life Sciences is preparing to sell its minority stake in the biopharmaceutical company Tubulis to Gilead Sciences. This strategic move is expected to generate a total value of up to $5 billion. The transaction highlights the growing interest by major firms in innovative therapeutic developments. Gilead Sciences aims to leverage Tubulis's advancements in biopharmaceuticals through this acquisition. The sale reflects EQT Life Sciences' approach to capitalizing on its investments in the life sciences sector. Both companies anticipate that this deal will accelerate the delivery of critical therapies to patients. As part of this transaction, EQT Life Sciences is expected to reallocate its resources towards new investment opportunities within the life sciences arena. The sale aligns with industry trends favoring the consolidation of innovative technologies in the biopharmaceutical space.

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