Assoc Clinical Development Director

Gilead SciencesUnited States - California - Foster Cityonsite$210k–$272kView the original posting at Gilead Sciences ↗

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 Associate Director, Virology Clinical Development (MD) The Associate Director, Virology Clinical Development (MD) plays a key role in the clinical development of therapies within the Virology Therapeutic Area. As a physician member of a multidisciplinary development team, this position contributes to the planning, execution, oversight, analysis, and reporting of clinical studies across multiple stages of development. The role provides scientific and medical expertise to support clinical development strategies, study conduct, regulatory submissions, data interpretation, and scientific communications. The successful candidate will collaborate closely with cross-functional partners and external stakeholders to help advance innovative treatments for patients with viral diseases. Location: Foster City, California This is an on-site, Foster City-based position. The successful candidate must work from the Foster City campus; remote work is not available for this role. This is an opportunity to contribute to the clinical development of novel therapies for HIV infection in a dynamic, collaborative environment. Working on-site as part of a cross-functional team, you will support the planning, execution, monitoring, and interpretation of clinical studies within the Virology Therapeutic Area. For assigned projects, you will contribute to a range of clinical trial activities, including study protocol development, investigator and study-related documentation, medical monitoring activities, data review and interpretation, study reporting, regulatory submissions, scientific publications, and presentations. This role provides an opportunity to gain broad experience across the clinical development process while helping advance innovative therapies for people with HIV. Key Responsibilities: Provides scientific and clinical expertise to cross-functional teams to support clinical development project deliverables and timelines. Contributes to the development and review of clinical trial protocols, clinical study reports, and responses to health authority inquiries. Provides ongoing medical monitoring for clinical trials, including but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance. Contributes to the clinical development component(s) in the preparation/review of regulatory documents, investigator brochures, and development plans. Supports the collection, review, and interpretation of clinical data for internal analysis and decision-making. Manages the preparation and/or review of data listings, summary tables, study results, and scientific presentations. Presents scientific and clinical information at investigator meetings, internal forums, and scientific conferences. Adheres to regulatory requirements of study conduct and industry standards of Good Clinical

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