* Supporting the receipt and processing of safety information: This can involve monitoring safety mailboxes, acknowledging receipt of adverse event reports, and ensuring proper documentation.
* Assisting with case processing: This may include initial data entry and following general data entry conventions.
* Recognizing different case types: Understanding which safety information requires expedited reporting to regulatory agencies.
* Collaborating with the drug safety operations team: Actioning and archiving emails and documents related to safety.
* Demonstrating basic knowledge of case management: Understanding the lifecycle of a safety report from receipt to submission.
* Assisting in the preparation of safety reports and other documentation: This could be for internal review or regulatory submissions.
* Conducting literature searches: As necessary for safety-related information.
* Supporting drug safety activities: Contributing to maintaining compliance with SOP and national/international regulations.