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 and aligning data science strategies with operational objectives, while ensuring compliance with regulations and quality standards. Proven ability to lead cross-functional teams, influence stakeholders, and drive process improvements in clinical development.

Highest-signal resume keywords

Clinical Trial ManagementProject ManagementData Science LeadershipRegulatory ComplianceOperational Analytics

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial ProcessesData ManagementProject Management ToolsOperational AnalyticsProcess Improvement

Soft Skills

Effective LeadershipInfluencing SkillsEffective CommunicationAnalytical Skills

Certifications & Qualifications

PMP CertificationLean Six Sigma Green Belt

Industry Keywords

PharmaClinical ResearchHealth CareGood Clinical PracticesICH Guidelines

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 single point of contact and accountable operational lead from DSS
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 program and study execution
Manage internal and external resources, track study progress, and prepare study status reports
Anticipate and resolve issues affecting timelines or quality
Ensure adherence to regulations, Good Clinical Practices, ICH Guidelines, AbbVie SOPs, and functional quality standards
Monitor evolving regulations, guidelines, and policies related to clinical development
Participate in vendor oversight and provide feedback on study operations and performance trends
Coach and mentor Data Science Associates
Participate in DSS and cross-functional 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 skills
Ability to influence others without direct authority
Effective communication skills
Effective analytical skills

Benefits

Comp & perks

Paid time off including vacation, holidays, and sick leave
Medical, dental, and vision insurance
401(k)
Short-term incentive programs
Flexible remote work arrangements
Coaching and mentoring opportunities