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The Pharmacovigilance Safety Scientist supports the Benefit Risk group by overseeing operational activities, authoring reports, ensuring quality standards, and validating data within regulatory compliance.

The Quality Lead oversees quality activities, controls SOPs, manages deviations and CAPAs, and ensures compliance with regulations. They support audits and drive continuous process improvement.

The Document Specialist is responsible for formatting and reviewing regulatory documents for electronic submissions, ensuring quality and compliance, and managing client expectations.

The Pharmacovigilance Intern will manage communication inboxes, assist with case processing in the Argus database, and ensure compliance with drug safety regulations.

The Data Analyst will enhance operational knowledge, develop reports, troubleshoot data issues, and support training while ensuring quality and confidentiality in all tasks.

The Talent Acquisition Partner will identify candidates for various roles, develop recruiting strategies, maintain applicant tracking, and manage recruitment processes in the pharmaceutical industry.