Data Science Program Lead I – Oncology

AbbVie

. Align DSS study teams with program- and study-level strategies .

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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading cross-functional study teams and managing clinical trials, ensuring adherence to regulations and quality standards. Proficient in operational analytics and project management to optimize study execution and resource management.

Highest-signal resume keywords

Clinical Trial ManagementProject ManagementOperational AnalyticsGood Clinical PracticesLeadership Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesData ManagementProject Management ToolsRegulatory ComplianceOperational Objectives

Soft Skills

Effective CommunicationInfluence Without AuthorityAnalytical SkillsCoaching and Mentoring

Certifications & Qualifications

PMP CertificationLean Six Sigma Green Belt

Industry Keywords

PharmaClinical ResearchHealth CareICH GuidelinesAbbVie SOPs

Tech Stack

Tools & technologies

PMP

About the role

Key responsibilities & impact

Align DSS 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, AbbVie 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 performance trends
Coach and mentor Data Science Associates
Provide indirect supervision of contract resources when applicable
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
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, influence without direct authority, communication, and analytical skills
Knowledge of federal and applicable local regulations, Good Clinical Practices, 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
Coaching and mentoring opportunities