Join Fortrea as an Associate II in Patient Safety Solutions, where you'll contribute to safety data management and adverse event processing. This role supports clinical trials and ensures compliance with safety regulations.

As an Associate II at Fortrea, you'll process and review adverse event reports while entering safety data and coding events using MedDRA. With over 2 years of pharmacovigilance experience, you'll ensure timely submissions of safety reports to regulatory bodies and clients. This position also involves collaboration with clients and mentoring team members to enhance safety protocols.

Key Responsibilities:
• Process adverse event reports from trials and post-marketing
• Enter safety data and write patient narratives
• Submit expedited safety reports to authorities
• Maintain tracking systems and project documentation
• Mentor team members and collaborate with clients

Requirements:
• Degree in Li...