Live opening · Posted 8 hours ago
At a glance
The key details from the original listing.
About the role
Description supplied by the original job listing.
Join Fortrea (sponsor-dedicated) and play a key role in the successful delivery of global clinical trials by providing essential operational and administrative support to study teams.
Key Responsibilities
Support the coordination and tracking of clinical trial activities and documentation.
Support the financial side of the projects.
Maintain Trial Master File (TMF) documentation and study tracking systems.
Coordinate study materials, supplies, and shipment logistics.
Assist with Investigator Meetings and project-related communications.
Collaborate with study teams, investigative sites, sponsors, and vendors.
Prepare reports and ensure accurate study records and data management.
Provide overall administrative support to clinical project teams.
What We're Looking For
Experience with finance and payments.
Strong written and verbal communication skills in English.
Previous administrative experience or exposure to the clinical research, pharmaceutical, or CRO industry is a plus.
Excellent organizational and time management abilities.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).
Detail-oriented with the ability to thrive in a fast-paced, matrix environment.
Learn more about our EEO & Accommodations request here.
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