Global Regulatory Start-Up Specialist — Clinical Trials
Listed on 2026-10-17
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Healthcare
Healthcare Compliance
CTI Clinical Trial and Consulting Services is seeking a regulatory professional to manage essential regulatory documentation for global clinical studies. You will support project teams, perform country-specific compliance assessments, and coordinate IRB/EC submissions with sponsors and sites.
The role requires 3–5 years of regulatory experience in pharma/CRO settings, with strong cross-functional collaboration and attention to detail. On-site work in Covington, KY is expected.
The Global Regulatory Start-Up Specialist — Clinical Trials role at CTI Clinical Trial and Consulting Services is now open for applications in Covington, KY, United States.
Step into the Global Regulatory Start-Up Specialist — Clinical Trials role at CTI Clinical Trial and Consulting Services in Covington, KY, United States and grow with us.
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If your experience matches this role, we encourage you to apply.
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