Clinical Data Strategy and Operations Program Lead III

📋 Description

• Lead and align CDSO study teams with program and study strategies.
• Coordinate CDSO study teams to meet operational objectives across programs.
• Engage global teams to support program and study objectives.
• Utilize analytics and PM tools to optimize execution and reporting.
• Ensure adherence to GCP, ICH, AbbVie SOPs, and local regs.
• Mentor team members and drive process improvement initiatives.

🎯 Requirements

• Bachelor’s in business, IT, life sciences; Master’s preferred. PMP or Lean Six Sigma Green Belt
• 8+ years pharma/clinical data experience or 10+ years PM experience.
• Deep understanding of clinical trial processes and stakeholders.
• Proven cross-functional leadership and coaching ability.
• Strong communication and analytical skills.

🎁 Benefits

• Regulatory compliance and quality assurance focus.
• Coaching and development opportunities for DS roles.
• Innovation and process improvement initiatives.
• Training needs assessment and standardization support.
• Vendors oversight and study performance trends.