TA Director, Risk Management Lead - Multiple Therapeutic Areas (Hybrid)

Tasks

• Collaborate with cross-functional stakeholders
• Coordinate risk based study modifications
• Develop risk insights dashboards
• Drive portfolio level risk identification
• Embed critical to quality into protocol design
• Ensure RAMP process accountability
• Implement risk mitigation plans
• Improve risk metrics and training
• Lead risk management lead team
• Oversee risk management strategy
• Standardize risk management best practices
• Track risk actions and monitoring

Perks/Benefits

• Hybrid work
• Local to Marlow required
• On site days T Th

Skills/Tech-stack

Clinical Practice | Clinical Trial Protocol Design | Clinical trial | Clinical trial protocol | Critical to quality | Data Visualization | Data analytics | EMA | Excel | FDA | Good Clinical Practice | ICH | 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 Management | Risk assessment and mitigation | Risk dashboards | Risk-Based Quality Management | Risk-based | Risk-based quality | Tableau