Associate Dir. Cross TA Risk Management
US026 PA Spring House - 1400 McKean Rd, United States
USD 122K-212K Mid-level Full Time
Tasks
- Communicate risk updates through governance forums
- Conduct risk monitoring reviews
- Coordinate identification assessment mitigation of quality risks
- Develop CAPA plans and effectiveness checks
- Drive inspection readiness activities
- Ensure consistent interpretation of quality investigation issues
- Maintain clinical quality plans in quality repository
- Provide guidance for significant quality issues
- Provide risk based clinical trial oversight
- Support investigator sponsor monitor and third party inspections
- Train and coach peers and new employees
Perks/Benefits
- 401k savings plan
- Hybrid work schedule
- Long-term incentive plan
- Retirement plan
- Sick time
- Vacation time
Skills/Tech-stack
CAPA | Clinical Practice | Clinical Quality Plan | Clinical Trial Risk Management | Clinical quality | Clinical trial | Clinical trials | Corrective and Preventive Action | Data Visualization | Data analytics | Effectiveness Check | Good Clinical Practice | Good Laboratory Practice | Good Manufacturing Practice | Good Pharmacovigilance Practice | ICH Guidelines | Laboratory practice | Preventive Action | Project Planning | Quality Plan | Risk Management | Spotfire | Tableau
Education
N/A
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