Microsoft Office (Word, Excel, Outlook) - advanced skills
Ability to communicate with all levels both verbally and written
Day to Day Responsibilities:
Support the compilation, submission and archiving of regulatory dossiers
Maintain regulatory document management systems and tracking systems
Maintain core dossier components
Quality control of regulatory dossiers, archive and tracking systems
Ensure the smooth compliant flow of regulatory information between all Functional areas, internal and external to GRAAS, local offices, external partners and regulatory authorities. To work with various functional areas to ensure health authority correspondence and submissions are maintained from planning through submission and ultimately approval.
No education requirement
"This posting is for Contingent Worker, not an FTE"