Senior Manager, QPPV Office

This is a fully remote position, open to applicants in Bulgaria, +3 more countries.

📋 Description

• Take charge of the pharmacovigilance agreement (PVA) management process.

• Supervise and ensure the prompt preparation of documents relevant to authorities.

• Design and create templates, project-specific documents, and processes.

⛳️ Requirements

• A minimum of two years of experience in global pharmacovigilance (excluding case processing), specifically in PVA management.

• Over four years of experience in pharmacovigilance, drug safety, epidemiology, risk management, scientific consulting, regulatory affairs, or a related discipline.

• A Bachelor's degree in life sciences, pharmacy, medicine, nursing, public health, epidemiology, regulatory affairs, or a related area, or equivalent experience is required.

• A certification in pharmacovigilance or drug safety is preferred.

• A certification in regulatory affairs or clinical safety is preferred.

• A certification in quality management or auditing is preferred.

🏝️ Benefits

• Benefit offerings outside the US may differ by country and will align with local market practices.

• Reasonable accommodations will be provided during the employment process for individuals with disabilities.