Clinical Safety Analyst - Remote

Overview

The Clinical Safety Analyst supports the Clinical Trial Patient Safety Organization to ensure the quality of clinical trial patient safety data through timely and accurate data review.

In Short

• Provides timely assessment of clinical trial data.
• Participates in safety surveillance activities.
• Maintains audit readiness for study deliverables.
• Monitors safety-related queries to Investigators.
• Collaborates with medical monitors on safety reviews.
• Creates narratives of serious adverse events.
• Stays current with ICH, FDA, and EMA guidance.
• Supports departmental process improvement projects.
• Delivers study-related information effectively.
• Aligns with AbbVie’s leadership behaviors.

Requirements

• Bachelor's degree in a related health science.
• 2+ years of clinical practice experience.
• RN or clinical pharmacy experience preferred.
• Drug safety experience with clinical trial management.
• Proficiency in Windows, Word, Excel, and databases.
• Ability to evaluate medical data critically.
• Effective communication skills.

Benefits

• Comprehensive benefits package including medical, dental, and vision insurance.
• 401(k) plan for eligible employees.
• Participation in short-term and long-term incentive programs.
• Paid time off for vacation, holidays, and sick leave.