Clinical Trials Manager

Role: Manage regional or small-scale clinical studies (primarily Phase I) within Gilead's clinical operations, focusing on study execution, vendor oversight, and regulatory compliance. Responsibilities: oversee study logistics, timelines, budgets, CRO/vendor interactions, and site management; contribute to study planning, protocol review, and reporting; ensure adherence to GCP, ICH, FDA, EMA regulations, and SOPs; collaborate with cross-functional teams and support training efforts. Requirements: MA/MS/PharmD/PhD with 3+ years or BA/BS/RN with 5+ years of relevant clinical or life sciences experience; demonstrated ability to manage study components and vendors; strong understanding of clinical trial regulations and best practices. Preferred: experience with early-phase studies, study management tools, and international regulatory standards; effective communication skills; ability to adapt across projects; willingness to travel as needed. High-Value: experience in Phase I trials, small or early-stage studies, regulatory compliance, vendor management, and working within Gilead's therapeutic areas. Work setup: global, with travel requirements, in a highly matrixed environment.