Diligent registered nurse with a background in direct patient care, documentation/transcription, and regulatory coordinating. Skilled in managing complex medical conditions and supporting patient recovery in fast paced environments. Demonstrating expertise in critical thinking and effective communication. Experience in offering comprehensive care in diverse populations.
Managing and supporting regulatory aspect of clinical trials, ensuring compliance with all applicable guidelines and regulations. Job tasks and responsibilities including, but not limited to study start up and close out, IRB submissions, informed consent review, amendment updates, safety reports, good clinical practice (GCP) guideline compliance, record keeping, and communication liaison between study team/principal investigator (PI)/sponsors.