- Lead the preparation submission maintenance:
- Clinical Trial Applications CTAs New Drug Submissions NDSs Supplemental NDSs SNDS lifecycle maintenance activities marketed products Review training materials advertising promotional content ensure compliance safety information report Tevas PV team Lead regulatory meetings Health Canada preCTA presubmission etc Serve Canadian regulatory lead global local project teams Monitor interpret intelligence assess impact evolving guidelines Ensure compliance regulations ICH guidelines internal SOPs Contribute process improvements best practices Regulatory Affairs function
Regulatory Affairs Manager - Montreal (administrative region) - Tevapharm
Description
The Opportunity
As Regulatory Affairs Manager at Teva Canada you will lead Canadian regulatory planning execution for innovative medicines biologics biosimilars small molecules.