Sr Regulatory Compliance Specialist

What you’d do

Leads and coordinates study-specific regulatory processes, including local IRB submissions and FDA communications, for clinical research studies across multiple therapeutic areas. Maintains documentation, case report forms, and study and regulatory files. Full time. Found on the employer's careers page on Oct 6, 2026. Apply through the link.

You’ll need

• Five years of experience in relevant research program experience
• Knowledge of Good Clinical Practices (GCP)
• Experience with IRB submissions
• Familiarity with FDA CFR and ICH regulations