Teams at Gilead Sciences

Leads the strategic, operational, financial, and regulatory oversight of oncology clinical trials and development programs. Manages cross-functional study teams, CROs, vendors, budgets, timelines, risk mitigation, trial documentation, SOPs, and local regulatory requirements. Provides therapeutic expertise, oversees clinical operations, supports protocol development, and communicates program status to stakeholders. May hire, coach, and develop team members.

Oversee clinical data management studies from start-up through close-out, ensuring data completeness, accuracy, quality, compliance, and timely deliverables. Lead eCRF design, query management, database snapshots, external data coordination, vendor deliverables, data transfer documentation, and cross-functional collaboration with Clinical Operations, Biostatistics, Programming, Safety, Regulatory, investigators, and study sites.

Supports global clinical data standards development, maintenance, governance, and study-level implementation. Applies CDISC standards, develops library objects and CRF guidelines, supports Medidata Rave EDC builds, performs quality checks, documents releases, and assists with change management and issue resolution. Collaborates with data management, programming, biostatistics, clinical operations, and governance committees to ensure consistent, compliant standards across clinical programs.