South San FranciscoFull TimeOther
Remotely
project managementdata managementregulatory compliancelean six sigmaclinical trialsdatapmp
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Job Description
📋 Description
- Lead CDSO study teams and represent DS in cross-functional teams.
- Coordinate CDSO study teams to meet operational objectives.
- Engage cross-functional teams to achieve program goals.
- Use operational analytics and PM tools to optimize execution.
- Monitor timelines, identify issues, and propose solutions.
- Ensure compliance with GCP, ICH, SOPs and regulatory standards.
🎯 Requirements
- Bachelor’s degree; Master’s preferred. PMP or Lean Six Sigma Green Belt desired.
- 3+ years pharma/clinical research or 5+ years PM experience.
- Strong understanding of clinical trial process and technology.
- Proven leadership and influencing skills.
- Excellent communication and analytical abilities.
🎁 Benefits
- Comprehensive benefits package including PTO and health insurance.
- Eligible for short-term incentive programs.
- Equal opportunity employer; relocations considered where applicable.