Site Readiness and Regulatory Specialist I
Fortrea
About this role
Entry-level role serving as the primary contact for investigative sites to support study maintenance and startup by ensuring collection of investigator and regulatory essential documents for timely EC/IRB/Regulatory Authority submissions. The position supports preparation and submission activities, communicates with internal and external stakeholders, and helps maintain study documentation and systems. It also involves developing awareness of country-specific regulatory legislation and guidance with support from senior staff.
Skills
Qualifications
About Fortrea
fortrea.comFortrea, a leading CRO, advancing clinical trials through patient-focused clinical solutions that accelerate clinical development, drive trial success, and bring innovative therapies to those who need them most.
Recent company news
Q4 Financial Peaks and Valleys: Comparing Fortrea (NASDAQ:FTRE) With Other Drug Development Inputs & Services Companies
3 hours ago
Q4 Earnings Highs And Lows: Fortrea (NASDAQ:FTRE) Vs The Rest Of The Drug Development Inputs & Services Stocks
19 hours ago
Fortrea Executive Shuffle Seeks Stronger Clinical Focus And Turnaround Potential
4 days ago
Fortrea Holdings Inc. (FTRE) 2026 Guidance Assumes Stable FX Rates from End-2025
2 days ago
Fortrea (NASDAQ:FTRE) Reports Sales Below Analyst Estimates In Q4 CY2025 Earnings
6 days ago
About Fortrea
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
Unlock Company Insights
View leadership team, funding history,
and employee contacts for Fortrea.
Salary
$61k – $81k
per year
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