Data Science Program Lead I – Oncology

atAbbVieRemoteUS flagNew JerseyFull-timeData ScientistSenior$84.5k – $162k/year

Posted 12 hours ago

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

πŸ“‹ Description

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

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

β€’ Serve as the primary point of contact for DSS and take accountability as the operational lead for assigned studies.

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

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

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

β€’ Utilize operational analytics and project management tools to enhance execution, manage resources, track study progress, and prepare status reports.

β€’ Anticipate and address potential issues impacting timelines or quality.

β€’ Ensure compliance with regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards.

β€’ Stay updated on evolving regulations, guidelines, and policies related to clinical development.

β€’ Participate in vendor oversight and offer feedback on study operations and performance trends.

β€’ Provide coaching and mentoring to Data Science Associates.

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

β€’ Engage in innovation and process improvement initiatives.

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


⛳️ Requirements

β€’ A 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 pharma, clinical research, data management, or healthcare, or 5 years of project management experience and/or relevant work experience.

β€’ Strong grasp of clinical trial processes and clinical technology.

β€’ Prior experience managing a clinical trial from initiation to completion is preferred.

β€’ Effective leadership skills, ability to influence without direct authority, excellent communication, and strong analytical abilities.

β€’ Familiarity with federal and applicable local regulations, Good Clinical Practices, ICH Guidelines, AbbVie SOPs, and functional quality standards.


🏝️ Benefits

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

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

β€’ 401(k) retirement plan.

β€’ Short-term incentive programs.

β€’ Option for remote work.

β€’ Opportunities for coaching and mentoring.

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