Regulatory Lead, Site
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Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
Job Description & How to Apply Below
K2 Medical Research in Maitland, FL is seeking a Regulatory Associate to manage site-level regulatory operations, IRB submissions, DOA logs, and study start-up compliance. This non-patient-facing, process-driven role requires meticulous timelines, strong eReg proficiency, and collaboration across departments to keep trials on track and compliant.
K2 offers medical, dental, and vision options, 401(k) with employer match, generous paid time off and holidays, and a four-day work week with 10-hour
We are currently recruiting a Regulatory Lead, Site Start-Up — 4-Day Week for our team in FL, United States.
Step into the Regulatory Lead, Site Start-Up — 4-Day Week role at K2 Medical Research in FL, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
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