Clinical Data Science Program Lead

AbbVie Inc.

Irvine (CA)

On-site

USD 85,000 - 162,000

Full time

2 days ago
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Benefits offered by this job

Paid time off
Medical/dental/vision insurance
401(k)
Short-term incentive programs

Job summary

AbbVie Inc. in Irvine, CA is seeking an experienced Data Science Program Lead to drive study-level execution and operational excellence within a cross-functional team.

You will align study strategies, coordinate DSS resources, manage timelines, and ensure adherence to GCP/ICH and AbbVie SOPs while mentoring junior staff. Ideal candidates bring 3+ years in pharma/clinical data and a proven ability to influence without direct authority, plus strong leadership, communication, and analytical skills.

Qualifications

  • Bachelor's degree in business, MIS, CS, or life sciences; Master’s preferred.
  • 3+ years pharma/clinical data experience or 5+ years project management experience.
  • Strong understanding of clinical trial processes and related technology.
  • Proven leadership and influence without authority.
  • Excellent communication and analytical skills.

Responsibilities

  • Aligns DSS study teams with program- and study-level strategies and leads the DSS Study Team.
  • Acts as single point of contact and operational lead; coordinates DSS study teams to meet objectives.
  • Engages cross-functional teams to achieve program and study goals.
  • Uses analytics and project tools to optimize execution, track progress, and report status.
  • Ensures compliance with GCP, ICH, AbbVie SOPs and local regulations.
  • Mentors Data Science Associates and oversees contract resources when needed.
  • Contributes to DSS and cross-functional process improvements.
  • Shares lessons learned across functions.

Skills

Leadership
Communication
Analytical skills
Project management
Stakeholder management

Education

Bachelor's degree
Master's degree

Job description

AbbVie Inc. in Irvine, CA is seeking an experienced Data Science Program Lead to drive study-level execution and operational excellence within a cross-functional team.

You will align study strategies, coordinate DSS resources, manage timelines, and ensure adherence to GCP/ICH and AbbVie SOPs while mentoring junior staff. Ideal candidates bring 3+ years in pharma/clinical data and a proven ability to influence without direct authority, plus strong leadership, communication, and analytical skills.

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