TA Director, Risk Management Lead - Multiple Therapeutic Areas (Hybrid)
North Chicago, IL, United States
USD 177K-336K (estimate) Executive-level Full Time
Tasks
- Collaborate with cross functional stakeholders on risk alignment
- Develop risk management best practices metrics and training
- Drive risk identification and mitigation strategies
- Embed critical to quality elements into protocol design
- Lead development and execution of therapeutic area risk insights
- Manage RAMP process accountability and timely risk action planning
- Oversee RAMP entry work and risk based study modifications
- Oversee clinical portfolio risk management strategy
Perks/Benefits
Skills/Tech-stack
Clinical Practice | Clinical Research | Clinical Trial Data | Clinical operations | Clinical trial | Clinical trial data analytics | Critical to quality | Dashboards | Data Risk | Data Visualization | Data analytics | Data risk management | EMA regulations | FDA Regulations | Good Clinical Practice | ICH GCP | ICH GCP E6 (R2) | Integrated Evidence Strategy | Mitigation planning | Protocol Design | Quality management | Ramp | Regulatory Compliance | Risk Assessment | Risk Assessment and Mitigation Planning | Risk Management | Risk assessment and mitigation | Risk-Based Quality Management | Risk-based | Risk-based quality
Education
Bachelor of Engineering | Bachelor of Science | Doctor of Medicine | Doctor of Pharmacy | Master of Science | Nursing Degree | PhD
Regions
Countries
States
Cities
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