- Amgen (Washington, DC)
- …Additionally, the Director will work cross-functionally with Global Patient Safety and Global Regulatory Affairs and Strategy at the leadership level to optimize ... background rates of events to inform signal evaluations, conducting post -approval safety studies globally (including post -marketing requirements, commitments,… more
- Stryker (Sacramento, CA)
- …+ 4+ years of industry experience in clinical, quality, or regulatory affairs (risk management, design quality, post -market safety, etc.), including 3 years ... in **Canada.** **What you will do** + Write/revise documents for regulatory submissions, pre-subs, annual reports, clinical evaluations, post -market clinical… more