Sr Director, Clinical Development; MD

Position: Sr Director, Clinical Development (MD)
* Lead execution of clinical trials and collaborations across the Respiratory and Emerging Viruses portfolio, working closely with senior leadership of the Respiratory and Emerging Viruses team.
* Ensure adherence to regulatory requirements of study conduct and industry standards of Good Clinical Practice.
* Coordinate the collection and analysis of clinical data for internal analysis and review.
* Serve as a key member of the team responsible for all scientific aspects of conceptualizing, planning, and executing trials.
* Lead or direct clinical trial protocol design and clinical study reporting for assigned molecules and products.
* Provide or oversee ongoing medical monitoring for clinical trials, including assessment of eligibility criteria, toxicity management, and drug safety surveillance.
* Oversee other Development Leads across the assigned project portfolio, as applicable.
* Serve as the lead for written and oral communications with health authorities.
* Lead, oversee, and direct the clinical development components of regulatory documents, investigator brochures, and development plans.
* Coordinate the collection and assimilation of data for internal analysis and review, and support preparation or review of data listings, summary tables, study results, and scientific presentations.
* Present scientific information at scientific conferences and clinical study investigator meetings; when applicable, take the lead in authoring scientific publications.
* Assist in the evaluation of business development opportunities.
* Adhere to regulatory requirements of study conduct, industry standards of Good Clinical Practice, and Gilead SOPs.
* Serve as a scientific and clinical resource within Gilead Clinical Research.
* Provide scientific and clinical guidance to Biology, Toxicology, Clinical Trials Management, Biometrics, Global Drug Safety, Regulatory, and Project Management teams.
* MD or equivalent with 8+ years of experience in drug development in industry, academia, or a related environment, working within cross‑functional project or program teams with proven success.
* Relevant experience in clinical research with a basic understanding of Good Clinical Practice.
* Experience in Infectious Diseases or Respiratory is preferred but not required.
* Ability to think analytically and strategically to formulate, develop, and execute clinical plans.
* Strong leadership skills with the ability to set vision, lead change, and mentor others.
* Ability to work effectively in a multidisciplinary team to cultivate an inclusive environment of respectful, open, and honest dialogue, fostering robust idea-sharing and creative problem solving.
* Excellent scientific written and oral communication skills.
* Ability to engage internal and external experts in constructive scientific and clinical dialogue regarding study design, study conduct, and interpretation of clinical results.
* Ability to travel domestically and internationally to company, scientific, regulatory, investigator, and other meetings.
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