Senior Clinical Safety Analyst – Pharmacovigilance Lead

Allergan; North Chicago (IL); On-site; USD 90,000 - 130,000; Full time

Job summary

AbbVie seeks a Senior Clinical Safety Analyst to independently review safety data from clinical trials, ensure regulatory compliance, and triage adverse events. The role collaborates with physicians, CROs, data management, and pharmacovigilance teams to ensure safety signals are identified and managed.

The successful candidate will interpret safety data, contribute to study reports, and support the department's SOPs while maintaining high-quality medical review standards.

Qualifications

• Bachelor's degree in health sciences is required; RN or clinical pharmacy experience preferred.
• Minimum clinical experience with drug safety/pharma experience as specified in ad.
• Proficiency in computer tools and databases used for safety data management.

Responsibilities

• Review safety data from clinical trials for quality and regulatory adherence.
• Triaging adverse events and coordinating with cross-functional teams.
• Supervise safety query tracking and communicate with investigators as needed.
• Assist with Safety Review Plan development and safety overviews for study teams.
• Create narratives for serious adverse events following regulatory standards.

Skills

Computer proficiency (Windows, Word,

Excel proficiency

Medical data evaluation

Adverse event interpretation

Task prioritization capability

Effective communication

Education

Bachelor's degree in health sciences

RN or clinical pharmacy experience preferred

Tools

Oracle/clinical databases

PIMS

Laboratory databases

Job description

AbbVie seeks a Senior Clinical Safety Analyst to independently review safety data from clinical trials, ensure regulatory compliance, and triage adverse events. The role collaborates with physicians, CROs, data management, and pharmacovigilance teams to ensure safety signals are identified and managed.

The successful candidate will interpret safety data, contribute to study reports, and support the department's SOPs while maintaining high-quality medical review standards.