Scientist, Drug Safety (Fixed Term)

Clinical Safety Scientist responsible for supporting safety reporting in clinical trials, assisting protocol lead in safety reporting activities, and collaborating with cross-functional colleagues.

Requirements

• Intake of reportable safety event information from clinical trial investigator sites
• Review, manage and create individual case safety reports for each event
• Ensure that all information required for a clinically complete and accurate case is present
• Generate safety queries to the trial investigator sites to ensure case report accuracy and completeness
• Prioritize daily work to ensure all events are submitted for entry into the safety database within the established timeframes
• Collaborate with cross-functional colleagues as needed
• Complete protocol-specific activities as required
• Actively participate and ensure effective communication with the protocol lead and other team members supporting their protocols
• Appropriately escalate protocol or individual event issues with other stakeholders, including CRAs/CRMs or protocol leads

Benefits

• VISA Sponsorship
• Flexible Work Arrangements