South San FranciscoFull TimeOther
Remotely
gcpproject managementdata managementlean six sigmaclinical trialsdatapmpich guidelines
Also available on
Job Description
📋 Description
- Lead CDSO study teams; represent DS on cross-functional study teams.
- Coordinate CDSO study teams to meet objectives; engage global teams.
- Influence cross-functional members to achieve program/study goals.
- Use operational analytics and PM tools to optimize study execution.
- Monitor timelines/quality; propose options to address issues.
- Ensure compliance with GCP, ICH guidelines, and AbbVie SOPs.
🎯 Requirements
- Bachelor’s in business, MIS, CS, life sciences; Master’s preferred.
- 3+ years pharma/clinical data or 5+ years PM experience.
- Strong clinical trial process understanding; end-to-end trial mgmt preferred.
- Demonstrated leadership and influencing abilities.
- Effective communication and analytical skills.
- PMP or Lean Six Sigma Green Belt desired.
🎁 Benefits
- Competitive compensation package; 401(k) plan.
- Paid time off and health benefits.
- Eligibility for short-term incentive programs.
