Specialist, Clinical Risk Management Oncology
Tasks
- Advise development of CAPA plans
- Assess clinical quality risks
- Coordinate identification of clinical quality risks
- Coordinate mock inspections
- Develop risk mitigation strategies
- Escalate significant quality issues
- Evaluate mitigation actions effectiveness
- Maintain clinical quality plans in quality repository
- Prepare inspection readiness activities
- Provide guidance on research quality and compliance
- Provide risk updates to R and D teams
- Review risk areas and track mitigation progress
- Support effectiveness checks
- Support investigator sponsor monitor and third party inspections
- Support serious breach evaluation
Perks/Benefits
- Annual bonus
- Bereavement leave
- Caregiver leave
- Parental leave
- Recognition awards
- Vacation days
- Volunteer leave
- Well-being reimbursement
Skills/Tech-stack
CAPA | Clinical Practice | Clinical risk management | Clinical trials | Compliance Management | Data Visualization | Data analytics | Good Clinical Practice | GxP | Health Authority Inspections | ICH Guidelines | Inspection Readiness | Microsoft Office | Project Management | Quality Assurance | Risk Management | Risk-Based Monitoring | Risk-based | Spotfire | Tableau
Education
N/A
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