IrvineFull TimeData Science
Remotely
leadershipgcpproject managementdata analyticsregulatory complianceclinical trialsdatasopsich guidelines
Also available on
Job Description
📋 Description
- Lead CDSO study teams; align with program and study strategies
- Act as single operational contact for CDSO studies
- Coordinate CDSO teams; engage global cross-functional groups
- Use analytics and PM tools to optimize execution and reporting
- Ensure compliance with GCP, ICH, SOPs and local regs
- Mentor Data Science Associates and oversee contract work if needed
🎯 Requirements
- Bachelor’s degree in business, MIS, CS, life sciences; Master’s preferred
- 3+ years pharma/clinical research experience or 5+ years PM experience
- Strong understanding of clinical trial process from startup to closeout
- Proven leadership and influencing skills
- Effective communication and analytical abilities
- PMP or Lean Six Sigma Green Belt desirable
🎁 Benefits
- AbbVie compensation and benefits package
- Short-term incentive eligibility
- Equal Opportunity Employer; relocation support may apply