Analyst

• Contribute to worldwide surveillance of clinical trial patient safety data and continuous improvement efforts
• Provide timely assessment of reported clinical trial data and participate in safety surveillance activities for assigned studies
• Review and analyze safety-related clinical trial data for content, quality, study-level trends, and adherence to regulatory guidance and protocols
• Maintain constant audit readiness for study deliverables
• Monitor safety-related queries to investigators
• Collaborate with the medical monitor to plan and execute study safety reviews
• Provide safety overviews to clinical teams, clinical research organizations, investigators, and investigator sites
• Participate in study protocol reviews to ensure appropriate safety language
• Review safety sections of clinical study reports and other ad-hoc safety reports
• Create narratives of serious adverse events and other events of interest according to accepted standards
• Serve on departmental process improvement projects as needed
• Support AbbVie’s strategic direction by demonstrating its “Ways We Work” leadership behaviors

Explore Clinical Safety Analyst at AbbVie. Review requirements and application details.

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