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gcp budgeting clinical operations cro asthma📋 Description
- Lead startup, execution, and closeout of COPD late-stage studies.
- Manage study budgets, timelines, and vendor relationships.
- Mentor junior team members and drive cross-functional collaboration.
- Coordinate with Data Management, Regulatory, and Clinical Operations.
- Oversee site activation, enrollment, monitoring, and data flow.
- Ensure GCP compliance and study document readiness.
🎯 Requirements
- Bachelor’s degree required; advanced scientific degree preferred.
- 8+ years in clinical operations; 4+ years in late-stage sponsor trials.
- Experience with CRO/vendor oversight and site management.
- Strong GCP knowledge; familiarity with FDA/EMA/MHRA regs.
- Excellent communication, collaboration, and mentoring skills.
- Willingness to travel up to 30% (domestic and international).
🎁 Benefits
- Annual bonus eligibility and equity compensation.
- Comprehensive benefits package.
- Flexible, collaborative work environment.
- Generous PTO and opportunities for growth.
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