different and innovative ways of seeing the world and solving problems. The Regulatory Coordinator II is part of our central... team providing regulatory support to Principal Investigators (PIs) and research study teams focused on mission-critical...
Responsibilities Prepare, track, and maintain all correspondence and regulatory documentation required by the IRB.... Submit all regulatory documents to the IRB and other governing bodies to maintain study compliance with GCP, institutional...
The Treuman Katz Center for Pediatric Bioethics and Palliative Care is hiring a clinical research coordinator II... regulatory documents; organizing protocol implementation and site initiation visits; and conducting routine monitoring...
different and innovative ways of seeing the world and solving problems. The Clinical Research Coordinator II (CRC II... operations of assigned research studies in accordance with study protocols, GCP guidelines, applicable regulatory requirements...
or other specialized training Clinical Research Coordinator II Minimum of two years full-time related experience in clinical research...: Clinical Research Coordinator I - $24.67 to $35.78 hourly Clinical Research Coordinator II - $28.85 to $42.98 hourly...
licensure or other specialized training Clinical Research Coordinator II Minimum of two years full-time related experience... Coordinator II - $28.85 to $42.98 hourly Benefits Medical, dental, vision insurance Flexible spending accounts: health care...
, GCP guidelines, applicable regulatory requirements and institutional policies. Coordinate patient enrollment... research or cancer registry environment with regulatory or human research protections. Knowledge of clinical trials records...
We are looking for a highly motivated and well-organized Clinical Research Coordinator Level 2 who possesses proven... processes and ensuring meticulous adherence to all relevant regulatory compliance requirements, with a strong ability to deliver...
of clinical research trials. Create and maintain regulatory documents; organize protocol implementation and site initiation visits...
of clinical research trials. Create and maintain regulatory documents; organize protocol implementation and site initiation visits...
using immunomagnetic selection. Troubleshoot and document problem specimens. Consult with the Coordinator as appropriate.../paperwork and processing logs appropriately. Review processing logs for accuracy and route to the Coordinator to resolve...