Global Clinical Program Lead

Regulatory Toolkit; Foster City (CA); Hybride; USD 165 000 - 236 000; Plein temps

Résumé du poste

Gilead Sciences Inc. is seeking a Clinical Program Manager to oversee worldwide Phase I–IV trials, manage study resources and budgets, and drive cross-functional execution.

The role emphasizes leadership across SMTs, adherence to SOPs, and collaboration with CROs within a hybrid on-site model in the Bay Area and other US locations. This position requires deep clinical operations expertise, regulatory knowledge, and strong program management with the ability to implement process improvements and

Qualifications

• BA/BS or RN with 8+ years’ relevant clinical or related experience in life sciences.
• MA/MS/PhD/PharmD with 6+ years’ relevant clinical or related experience in life sciences.

Responsabilités

• Provides ongoing financial oversight of clinical trials/programs assigned.
• Leads cross-functional Study Management Teams (SMTs) and influences all relevant stakeholders.
• Partners with cross-functional teams to manage timelines and budgets as needed.
• Communicates project status and issues to ensure goals are met.

Connaissances

Cross-functional leadership

Study management

Budget oversight

Regulatory knowledge

Formation

BA/BS or RN

Advanced degree (MA/MS/PhD/PharmD)

Description du poste

Gilead Sciences Inc. is seeking a Clinical Program Manager to oversee worldwide Phase I–IV trials, manage study resources and budgets, and drive cross-functional execution.

The role emphasizes leadership across SMTs, adherence to SOPs, and collaboration with CROs within a hybrid on-site model in the Bay Area and other US locations. This position requires deep clinical operations expertise, regulatory knowledge, and strong program management with the ability to implement process improvements and