Senior Clinical Data Strategy & Ops Program Lead III

Allergan; South San Francisco (CA); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie Data Science is seeking an experienced program leader to align CDSO study teams with strategic objectives, coordinating global cross-functional efforts to ensure timely delivery and quality of clinical data initiatives.

This role requires 8+ years in pharma/clinical data management or 10+ years project management, with strong governance, communication, and analytical skills to drive program success across regulatory and quality standards.

Qualifications

• Bachelor’s degree in business, MIS, CS, life sciences or equivalent; Master’s preferred; PMP or Lean Six Sigma Green Belt desired.
• 8+ years pharma/clinical research/data management or 10+ years project management experience.
• Understanding of clinical trial processes and stakeholder management; lead role in trials.
• Cross-functional leadership and ability to influence without direct authority; strong communication and analytical skills.

Responsibilities

• Aligns CDSO study teams with program- and study-level strategies and governance.
• Acts as single point of contact and operational lead from CDSO for assigned programs.
• Coordinates CDSO teams across global functions to meet objectives.
• Interacts with management and cross-functional members to achieve program goals.
• Lead CDSO and cross-functional innovation and process improvements.

Skills

Pharma/clinical experience

Cross-functional leadership

Regulatory knowledge

Analytical skills

Education

Bachelor’s degree in business/IT/life sciences

Master’s degree preferred

PMP or Lean Six Sigma Green Belt desired

Tools

Project management tools

Job description

AbbVie Data Science is seeking an experienced program leader to align CDSO study teams with strategic objectives, coordinating global cross-functional efforts to ensure timely delivery and quality of clinical data initiatives.

This role requires 8+ years in pharma/clinical data management or 10+ years project management, with strong governance, communication, and analytical skills to drive program success across regulatory and quality standards.