Data Science Program Lead I – Oncology

🕒 6 days ago

🌽 Illinois – Remote

🌽 Illinois – Remote

💵 $84.5k - $162k / year

⏰ Full Time

🟠 Senior

📊 Data Scientist

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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

🏥 Healthcare

💼 Consulting

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Healthcare • Consulting • Manufacturing

AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.

📋 Description

• 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 program and study execution • Manage internal and external resources, track study progress, and prepare study status reports • Anticipate and identify issues affecting timelines or quality and develop solutions • Ensure adherence to federal and local regulations, GCPs, ICH Guidelines, AbbVie SOPs, and functional quality standards • Stay current on regulations, guidelines, and policies related to clinical development • Participate in vendor oversight and provide feedback on study operations, issues, and performance trends • Coach and mentor Data Science Associates • Provide indirect supervision of contract resources as needed • Participate in DSS and cross-functional innovation and process improvement initiatives • Contribute study execution lessons learned across functions

🎯 Requirements

• 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 process and clinical technology • Experience managing a clinical trial from initiation through completion preferred • Demonstrated effective leadership skills • Ability to influence others without direct authority • Demonstrated effective communication skills • Demonstrated effective analytical skills

🏖️ Benefits

• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Eligibility to participate in short-term incentive programs

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