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Regulatory Coordinator II - Clinical Trial Office
Brookline or Maine or Vermont or New Hampshire or Massachusetts or Connecticut or Rhode Island
$61k-$68k/yr HybridFull Time
1+ YOECompletes regulatory submissions and tracking for clinical trials (IND/IDE, IRB, FDA), maintains regulatory files, coordinates study start-up, and ensures compliance with FDA and ICH/GCP; requires bachelor’s degree or equivalent experience and 1–3 years regulatory experience.
Microsoft applications, databases
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Clinical Research
Wakefield, Rhode Island, United States
$16-$20/hr OnsiteFull Time
Bachelor's in human health care, EMR and Microsoft Suite proficiency, knowledge of IRB/GCP/HIPAA, strong computer and communication skills, ability to coordinate clinical trials and manage study data.
Electronic Medical Records (EMR), EMR Systems, Practice Management System, Microsoft Outlook, Microsoft Word, Microsoft Excel
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Monitoring Excellence Academy - OMEA - Oncology / CAR T & Gen Meds - CRA 1
United States or Rhode Island or Michigan or California or Florida or Arizona or Nevada or Oregon or Massachusetts or New Mexico or Kansas or North Dakota or South Dakota or Ohio or Illinois or Oklahoma or Utah or New York or Missouri or Tennessee or Idaho or New Jersey or Washington or Wisconsin or Montana or Texas or Montreal or Colorado or Indiana or Maine or Durham
$80k-$90k/yr RemoteFull Time
2+ YOE2+ years as a study coordinator or research nurse in oncology/CAR T/Gen Meds; university/college degree or allied health certification; able to travel 60-70% overnight; strong clinical judgment and teamwork.