Jobs at ProPharma

Oversee daily processing of adverse event cases, conduct peer reviews, mentor staff, and ensure compliance with global safety regulations. Provide client notifications and create training materials for pharmacovigilance processes.

The Workday Technical Developer is responsible for integrating solutions within Workday, requiring collaboration with teams to gather requirements, maintain existing integrations, and manage the development life cycle.

Coordinate and monitor the Quality & Compliance Audit Program, support Global Audit Coordination Sr. Manager, Project Managers, and Sponsors. Generate and manage contract documents, set up audits in DOT and Workday, review time/expenses and invoices, maintain audit tracking logs and project reports, ensure documentation meets SOPs/client requirements, and provide administrative support for large audit projects.

The Pharmacovigilance Scientist will support safety documentation and regulatory outputs, author safety reports, maintain risk management plans, and ensure compliance with regulatory requirements.

The Pharmacovigilance Specialist focuses on adverse event submission compliance, operational support in Argus, and periodic reporting for pharmacovigilance processes.