Data Science Program Lead I – Oncology

AbbVie

. Align Data and Statistical Sciences study teams with program- and study-level strategies .

Posted 10/22/2026full-timeRemote • California • United StatesSenior💰 $84,500 - $162,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trials, ensuring adherence to regulations and quality standards, while effectively leading cross-functional teams and optimizing project execution through operational analytics.

Highest-signal resume keywords

Clinical Trial ManagementProject ManagementGood Clinical Practices (GCPs)PMP CertificationData Science Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Operational AnalyticsProject Management ToolsClinical TechnologyData ManagementProcess Improvement

Soft Skills

Effective LeadershipInfluencing SkillsCommunication SkillsAnalytical Skills

Certifications & Qualifications

PMP CertificationLean Six Sigma Green Belt

Industry Keywords

Clinical ResearchPharmaceuticalsICH GuidelinesSOPsRegulatory Compliance

Tech Stack

Tools & technologies

PMP

About the role

Key responsibilities & impact

Align Data and Statistical Sciences study teams with program- and study-level strategies
Lead DSS Study Teams and represent Data Science on cross-functional study teams
Serve as the DSS single point of contact and accountable operational lead for assigned studies
Coordinate DSS study teams to meet operational objectives
Engage and connect global functional and cross-functional teams
Influence cross-functional team members to achieve program and study objectives
Use operational analytics and project management tools to optimize execution, manage resources, track study progress, and prepare status reports
Anticipate and resolve issues affecting timelines or quality
Ensure adherence to regulations, GCPs, ICH Guidelines, SOPs, and quality standards
Monitor evolving regulations, guidelines, and policies related to clinical development
Participate in vendor oversight and provide feedback on study operations and vendor performance
Coach and mentor Data Science Associates, with possible indirect supervision of contract resources
Participate in innovation and process improvement initiatives
Contribute study-execution lessons learned across functions

Requirements

What you’ll need

Bachelor's degree in business, management information systems, computer science, life sciences, or equivalent
Master's degree preferred
PMP Certification or Lean Six Sigma Green Belt desired
At least 3 years of pharma, clinical research, data management, or health care experience, or 5 years of project management experience and/or applicable work experience
Strong understanding of clinical trial processes and clinical technology
Experience managing a clinical trial from initiation through completion preferred
Effective leadership, influencing, communication, and analytical skills
Knowledge of federal and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie SOPs, and functional quality standards

Benefits

Comp & perks

Paid time off, including vacation, holidays, and sick leave
Medical, dental, and vision insurance
401(k)
Short-term incentive programs
Remote work option
Equal opportunity employer benefits and reasonable accommodation support