TA Director, Risk Management Lead - Multiple Therapeutic Areas (Hybrid)
USD 177K-336K (estimate) Executive-level Full Time
Tasks
- Collaborate with clinical site management clinical study leadership data science and compliance
- Drive portfolio risk identification and mitigation strategies
- Embed critical to quality elements into protocol design
- Ensure RAMP process accountability
- Implement risk based modifications to study scope
- Lead develop and mentor risk management leads team
- Oversee RAMP entry work
- Oversee risk insights dashboards and mitigation plans
- Standardize and improve risk management best practices metrics and training
- Track risk actions and planning timelines
Perks/Benefits
Skills/Tech-stack
Clinical Practice | Critical to quality | Data Visualization | Data analytics | Excel | Good Clinical Practice | ICH GCP | ICH GCP E6 (R2) | Mitigation planning | Power BI | Protocol Design | Quality management | RBQM | Ramp | Regulatory Compliance | Risk Assessment | Risk Assessment and Mitigation Planning | Risk assessment and mitigation | Risk-Based Quality Management | Risk-based | Risk-based quality | Tableau
Education
Bachelor of Science | Doctor of Medicine | Master of Science | PhD | PharmD
Regions
Countries
States
Cities
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