Data Science Program Lead I – Oncology

atAbbVieRemoteUS flagIllinoisFull-timeData ScientistSenior$84.5k – $162k/year

Posted 12 hours ago

This is a fully remote position, open to applicants in Illinois.

πŸ“‹ Description

β€’ Align DSS study teams with program- and study-level strategies.

β€’ Lead DSS Study Teams and act as the representative for Data Science on cross-functional study teams.

β€’ Serve as the designated point of contact and operational lead for the assigned studies within DSS.

β€’ Coordinate DSS study teams to achieve operational goals.

β€’ Engage and foster connections among global functional and cross-functional teams.

β€’ Influence members of cross-functional teams to meet program and study objectives.

β€’ Utilize operational analytics and project management tools to enhance program and study execution.

β€’ Manage both internal and external resources, monitor study progress, and create study status reports.

β€’ Anticipate and identify challenges impacting timelines or quality, and devise solutions.

β€’ Ensure compliance with federal and local regulations, GCPs, ICH Guidelines, AbbVie SOPs, and functional quality standards.

β€’ Stay informed on regulations, guidelines, and policies pertinent to clinical development.

β€’ Participate in vendor oversight and provide insights on study operations, issues, and performance trends.

β€’ Coach and mentor Data Science Associates.

β€’ Offer indirect supervision of contract resources as necessary.

β€’ Engage in DSS and cross-functional innovation and process improvement initiatives.

β€’ Share lessons learned from study execution across functions.


⛳️ Requirements

β€’ Bachelor's degree in business, management information systems, computer science, life sciences, or a related field.

β€’ A Master's degree is preferred.

β€’ PMP Certification or Lean Six Sigma Green Belt is desirable.

β€’ A minimum of 3+ years of experience in pharmaceuticals, clinical research, data management, or healthcare, or 5+ years of project management and/or relevant work experience.

β€’ Strong knowledge of the clinical trial process and clinical technology.

β€’ Preferred experience in managing a clinical trial from initiation to completion.

β€’ Proven leadership abilities.

β€’ Capability to influence others without direct authority.

β€’ Demonstrated strong communication skills.

β€’ Proven analytical skills.


🏝️ Benefits

β€’ Paid time off (including vacation, holidays, and sick leave).

β€’ Medical, dental, and vision insurance coverage.

β€’ 401(k) retirement plan.

β€’ Eligibility to participate in short-term incentive programs.

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