Data Science Program Lead – Clinical Trials Ops

BioSpace; South San Francisco (CA); Presencial; USD 120.000 - 180.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Comprehensive benefits package

Short-term incentive program

401(k) plan

Descripción de la vacante

AbbVie is seeking a Strategic CDSO Lead in California to drive study execution in Clinical Data Strategy and Operations. You will coordinate cross-functional teams, manage operational risks, and align study objectives with program strategies.

This role emphasizes leadership, data-driven decision making, and regulatory compliance across trials. The position requires pharma/clinical research experience or strong project management background, with a focus on collaboration and process improvement

Formación

• Bachelor’s degree in business, management information systems, computer science, life sciences or equivalent.
• Master’s degree preferred for advancement and leadership roles.
• Experience in pharma/clinical research or data management is required or highly beneficial.

Responsabilidades

• Aligns CDSO study teams with program- and study-level strategies and leads the CDSO Study Team.
• Acts as single point of contact and operational lead from DSS for assigned studies.
• Coordinates DSS study teams to meet objectives and connects global teams across the organization.
• Uses analytics and project management tools to optimize study execution and resource management.
• Ensures compliance with FDA/ICH regulations, GCPs, SOPs, and internal quality standards.
• Mentors Data Science Associates and may supervise contract resources.

Conocimientos

Project leadership

Cross-functional leadership

Analytical skills

Communication skills

Regulatory knowledge

Stakeholder management

Educación

Bachelor’s degree in relevant field

Master’s preferred

Descripción del empleo

AbbVie is seeking a Strategic CDSO Lead in California to drive study execution in Clinical Data Strategy and Operations. You will coordinate cross-functional teams, manage operational risks, and align study objectives with program strategies.

This role emphasizes leadership, data-driven decision making, and regulatory compliance across trials. The position requires pharma/clinical research experience or strong project management background, with a focus on collaboration and process improvement