Associate Director, Patient Safety- Virology

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.Job SummaryThe Associate Director, Patient Safety-Virology provides strategic pharmacovigilance leadership for one or more products, compounds, or indications across the development and/or post‑marketing lifecycle. This role contributes safety expertise to ensure continuous evaluation of benefit–risk profiles, regulatory compliance, and patient safety, while serving as a key Patient Safety representative on cross‑functional teams.The Associate Director operates with a high level of autonomy, partnering across functions to support product development, lifecycle management, and post‑authorization safety activities.Key ResponsibilitiesProvide scientific input into pharmacovigilance activities, including safety surveillance, signal detection and evaluation, and benefit–risk assessments for assigned products and assisting with pharmacovigilance activities for other products when neededContribute to the development and execution of safety strategies across the product lifecycle from clinical development through post‑marketingProvide input into aggregate safety reports (e.g., PSURs/PBRERs, DSURs), regulatory submissions, and responses to health authority inquiriesSupport risk management activities, including Risk Management Plans, risk minimization measures, and safety‑related labeling updates.Contribute to activities related to regulatory filings and responses to safety queries from third parties, such as regulatory agencies, as neededReview of clinical study protocols, amendments, and study‑related documentsRepresent Patient Safety on cross‑functional teams, collaborating with Clinical Development, Regulatory Affairs, Medical Affairs, RWE/HEOR, and other functionsEnsure pharmacovigilance activities are conducted in compliance with global regulations, internal SOPs, and quality standardsContribute to inspection readiness, process improvement initiatives, and the ongoing enhancement of Patient Safety operating modelsBuild effective working relationships and provide thoughtful safety input to internal stakeholders to support patient‑centric decision‑makingEducation and Experience RequirementsPharmD/PhD with 2+years’ relevant experience.MA/MS/MBA with 8+ years’ relevant experience.BA/BS with 10+ years’ relevant experience.Relevant experience in pharmacovigilance / patient safety within the pharmaceutical or biotechnology industryWorking knowledge of global pharmacovigilance regulations and aggregate safety reporting requirementsDemonstrated ability to evaluate safety data, apply clinical judgment, and communicate benefit–risk considerationsExperience working effectively in cross‑functional, matrix environments.Preferred QualificationsExperience supporting safety oversight for products across multiple stages of the development or post‑marketing lifecyclePrior involvement in safety signal evaluation, risk management activities, and regulatory interactionsStrong written and verbal communication skills with the ability to present complex safety information to diverse stakeholdersAbility to manage multiple priorities and products concurrently in a fast‑paced environmentPeople Leader Accountabilities: Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams. Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose. Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.  The salary range for this position is: $195,670.00 - $253,220.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.F