Clinical Safety and Risk Management Associate Principal Scientist

The Clinical Safety and Risk Management Associate Principal Scientist performs primary medical review of serious adverse experience reports and other AE reports of interest in order to monitor and describe the safety profile of assigned products. Assists in the oversight and development of pharmacovigilance and risk management plans.

Requirements

• At least two years of clinical experience in a patient care setting is required
• Minimum 5 years of professional experience with both clinical and pharmaceutical industry experience required
• Experience in drug safety, pharmacovigilance and/or risk management
• Excellent writing and communication skills in English
• Demonstrated leadership skills in managing programs, processes, and facilitating meetings

Benefits

• VISA Sponsorship