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gcpproject managementlean six sigmadatapmpregulatoryclinical dataich guidelines
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Job Description
📋 Description
- Aligns CDSO study teams with program- and study-level strategies
- Serves as single point of contact and operational lead from CDSO for assigned studies
- Coordinates CDSO study teams to meet objectives; connects global teams
- Uses operational analytics and tools to optimize program execution
- Tracks study progress and prepares status reports
- Ensures adherence to GCP, ICH Guidelines, AbbVie SOPs and local regs
🎯 Requirements
- Bachelor’s degree in business, MIS, CS, life sciences; Master’s preferred
- PMP or Lean Six Sigma Green Belt desired
- 3+ years pharma/clinical research/data management or 5+ years PM experience
- Strong understanding of clinical trial processes and tech
- Proven leadership and ability to influence without authority
- Effective communication and analytical skills
🎁 Benefits
- We offer compensation; see posting for details
- Comprehensive benefits package (time off, health, 401(k))
- Eligible for short-term incentive programs
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