Data Science Program Lead I – Oncology

🔥 12 minutes ago

🏄 California – Remote

🏄 California – Remote

💵 $84.5k - $162k / year

⏰ Full Time

🟠 Senior

📊 Data Scientist

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

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 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

• 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

• 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