Associate II, Patient Safety Solutions Client Dedicated Toronto, Canada

The Associate II Patient Safety Solutions will manage adverse event reporting and ensure compliance with regulatory timelines.

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:

• Work is performed in an office environment with exposure to electrical office equipment.

• Occasional drives to site locations with occasional travel both domestic and international.

Physical Requirements:

• Frequently stationery for 6-8 hours per day.

• Repetitive hand movement of both hands with the ability to make fast simple repeated movements of the fingers hands and wrists.

• Occasional crouching stooping with frequent bending and twisting of upper body and neck.

• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

• Regular and consistent attendance.

• Varied hours may be required.

Learn more about our EEO & Accommodations request here.