Experteer Overview In this Clinical Operations role, you will oversee global Phase I–IV trials through site identification, enrollment planning, and study execution. You will serve as the main liaison between investigator sites and Gilead Development, driving collaboration to deliver high-quality data and timely milestones. You will nurture a network of preferred sites and escalate issues to remove barriers to trial progression. This position offers the chance to shape site strategy, optimize partnerships, and contribute to global registration and patient access.Compensaciones / Beneficios
- Establish and maintain strong relationships with investigator sites to optimize trial delivery
- Develop strategies to provide concierge-level support for preferred sites and become Sponsor of Choice
- Track site performance metrics and identify opportunities for improvement
- Identify new investigator sites aligned with portfolio strategy to expand the research network
- Maintain therapeutic and technical expertise for scientific discussions with sites
- Share development pipeline updates and gather field intelligence impacting trials
- Support study teams and CROs to ensure timely trial delivery from start-up to closeout
- Collect site feedback and insights to inform internal improvements
- Develop and implement site risk plans to meet key milestones and enrollment commitments
- Escalate issues at investigator sites and coordinate mitigations with internal teams
- Present metrics to inform site/country/regional decision making
- Build local knowledge of site capabilities for recruitment forecasts and monitoring
- Collaborate with Clinical Operations, Clinical Development, and Medical Affairs for unified messaging
- Champion patient perspectives across product development based on insights from PAGs and communitiesResponsabilidades
- BA/BS/RN with 10+ years in life sciences OR MA/MS/PharmD/PhD with 8+ years in life sciences
- Strong clinical operations knowledge across Oncology, Virology, Inflammation a plus
- Solid understanding of Good Clinical Practice and regulatory guidelines
- Strong self-management and organizational skills
- Ability to work independently and in teams
- Excellent verbal and written communication and presentation skills in English and local language
- Ability to build long-term relationships with internal and external stakeholders
- Strong interpersonal skills and team-focused mindset
- Leadership presence with ability to influence without authority
- Strong negotiation, conflict resolution, strategic agility and business acumen
- Willingness to travel extensivelyRequisitos principales
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