Phase Clinical Start-Up Specialist - Regulatory & Site Activation
Listed on 2026-10-03
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Healthcare
Fortrea seeks a Study Start Up Specialist in the United States to coordinate regulatory submissions and collect essential documents for site activation and ongoing maintenance. You will ensure compliance with EC/IRB/Regulatory Authority requirements, track timelines, and act as a local expert across start-up activities.
This role involves mentoring teammates, drafting country applications, and collaborating with vendors to prepare audit-ready documentation in a fast-paced, technology-driven
This posting is for the Phase I Clinical Start-Up Specialist - Regulatory & Site Activation role at Fortrea, based in United States.
The position is based in United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 50.000 - 70.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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