Data Science Program Lead I – Oncology

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

Posted 12 hours ago

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

πŸ“‹ Description

β€’ Align study teams within Data and Statistical Sciences with the strategies at both program and study levels.

β€’ Take the lead of DSS Study Teams and represent Data Science on interdisciplinary study teams.

β€’ Act as the DSS primary point of contact and the accountable operational leader for assigned studies.

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

β€’ Foster engagement and connectivity among global functional and cross-functional teams.

β€’ Influence members of cross-functional teams to achieve program and study goals.

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

β€’ Proactively identify and address issues that may impact timelines or quality.

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

β€’ Keep abreast of evolving regulations, guidelines, and policies related to clinical development.

β€’ Engage in vendor oversight and provide insights on study operations and vendor performance.

β€’ Mentor and coach Data Science Associates, potentially overseeing contract resources indirectly.

β€’ Contribute to innovation and initiatives for process improvement.

β€’ Share lessons learned from study execution across different 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 desired.

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

β€’ A strong comprehension of clinical trial processes and clinical technology.

β€’ Experience in managing a clinical trial from initiation to completion is preferred.

β€’ Excellent leadership, influencing, communication, and analytical skills.

β€’ Familiarity with federal and applicable local regulations, Good Clinical Practices (GCPs), 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.

β€’ 401(k) plan.

β€’ Short-term incentive programs.

β€’ Option for remote work.

β€’ Benefits as an equal opportunity employer and support for reasonable accommodations.

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