Key Responsibilities:

• Process and review adverse event reports from clinical trials and post-marketing sources.
• Enter safety data, write patient narratives, and code events using MedDRA.
• Ensure timely submission of expedited safety reports to regulatory authorities and clients.
• Maintain tracking systems, project documentation, and support audits and inspections.
• Collaborate with clients and mentor team members as needed.

What you need to bring:

• Degree in Life Sciences or related field preferred.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• 2+ years of pharmacovigilance or safety experience.
• Strong attention to detail, communication skills, and ability to work independently.
• Proficiency in MS Office and safety databases.

Note:

This role does not provide sponsorship.

Work Environment:...