Senior Patient Safety Manager

Role Overview

Lead global and/or regional pharmacovigilance processes across Sandoz business units, ensuring compliance with worldwide regulations and maximum efficiency. Responsible for compliance, quality, efficiency, and management of Post Marketing and Clinical Trial adverse event handling.

What You Will Do

Monitor and audit the company's drug, biologics, or medical devices surveillance program, including intake, evaluation, processing, and follow-up on adverse reports. Provide trending and safety signal detection and assessment. Support all clinical trial activity and post-marketing.

Why It Might Be a Fit

Ideal candidate will have experience in pharmacovigilance, clinical trials, and team management. Strong leadership and communication skills are required to build high-performance safety teams and manage direct reports.

Requirements

• Work Experience: Critical Negotiations, People Challenges, Operations Management and Execution, Collaborating across boundaries, People Leadership
• Skills: Clinical Trial, Databases, Employee Training, Pharmacovigilance, Project Management, Reporting, Safety Science, Team Management

Benefits

• Equal Opportunity Employer
• Reasonable Accommodation for individuals with disabilities