A company is looking for a Regulatory Affairs Senior Associate to support regulatory document management and clinical trial submissions.
Key ResponsibilitiesMaintain regulatory document management and tracking systemsSupport activities for clinical trial and marketing application submissions and health authority correspondenceCollaborate with external partners and manage submissions related to protocol amendments and investigator updatesQualifications & Requirements1-2 years of regulatory experienceExperience with SharePoint, Excel, Smartsheet, and Veeva VaultAbility to work independently and manage multiple prioritiesExperience in providing training and support to team membersFamiliarity with compliance to SOPs and regulatory authorities
Associate Director Regulatory Affairs
A company is looking for an Associate Director, Regulatory Affairs and Submissions. ...
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