Pharma Admin
Skills
About This Role
Overview
- Manage and maintain pharmaceutical regulatory documentation, ensuring compliance with global standards and guidelines.
- Coordinate and track clinical trial activities, including data entry, patient enrollment support, and communication with investigators.
- Provide administrative support for pharmacovigilance activities, such as adverse event reporting and safety data management.
- Assist in the preparation and submission of regulatory filings to health authorities, ensuring accuracy and timeliness.
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