Regulatory Strategist III - Sanford
Only for registered members Sanford, United States
1 week ago
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Job summary
This position requires regulatory experience with a highly preferred background in vaccines and documentation management.
+Responsibilities
- Prepare/author regulatory sections for clinical trial applications and amendments, registration dossiers, annual reports and post-approval variations and renewals.
- Develop regulatory post-approval filing strategies and variations for global products.
Skills
- Regulatory exp. is a must with a HIGHLY preferred background in vaccines
,valid_job:1}
Job description
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