Data Science Program Lead — Clinical Trials Strategy

Data Business GmbH

North Chicago (IL)

On-site

USD 120,000 - 170,000

Full time

14 days+

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Benefits offered by this job

Benefits package
401(k) plan
Paid time off

Job summary

AbbVie is seeking a Clinical Data Strategy and Operations lead to align study teams with program strategies and coordinate global teams. You will drive operational execution, ensure regulatory compliance and mentor data science associates while contributing to process improvements across CDSO and cross-functional initiatives.

The role requires 3+ years pharma/clinical research experience or 5+ years project management, plus strong leadership and communication skills and a solid understanding of

Qualifications

  • 3+ years pharma/clinical research/data management/healthcare experience or 5+ years PM experience.
  • Strong understanding of the clinical trial process and clinical technology.
  • Ability to influence others and lead cross-functional teams.
  • Effective communication and analytical skills.

Responsibilities

  • Aligns CDSO study teams with program- and study-level strategies.
  • Acts as single point of contact and operational lead from DSS for studies.
  • Coordinates DSS study teams to meet objectives and connects global teams.
  • Uses analytics and PM tools to optimize program execution and track progress.
  • Ensures adherence to GCP, ICH, SOPs and regulatory requirements.
  • Mentors Data Science Associates and may supervise contract resources.
  • Contributes to CDSO and cross-functional innovation initiatives.
  • Shares lessons learned across functions.

Skills

Leadership
Communication
Analytical skills
Project management

Education

Bachelor’s degree in business, MIS, CS, life sciences or equivalent
Master’s degree preferred
PMP or Lean Six Sigma Green Belt desirable

Job description

AbbVie is seeking a Clinical Data Strategy and Operations lead to align study teams with program strategies and coordinate global teams. You will drive operational execution, ensure regulatory compliance and mentor data science associates while contributing to process improvements across CDSO and cross-functional initiatives.

The role requires 3+ years pharma/clinical research experience or 5+ years project management, plus strong leadership and communication skills and a solid understanding of

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