RN, Clinical Research Coordinator

FlexStaff is hiring a Clinical Research Coordinator, RN for our client, a cutting-edge cancer treatment center. In order to qualify, you must possess an active NY State RN license . As a Clinical Research Coordinator (CRC, RN), you will provide essential support to senior research staff, contributing to the daily operations of early-phase oncology clinical trials. You will ensure the accurate and timely conduct of research, strictly adhering to study protocols, regulatory guidelines, and patient safety standards.

Key responsibilities include :

• Direct patient interaction, meticulous data collection, and maintaining rigorous compliance with Good Clinical Practice (GCP).
• Managing a portfolio of multiple protocols, you will plan and coordinate patient participation, overseeing all aspects of the trial process.
• You will be responsible for the timely implementation and completion of all protocol-specific requirements, serving as a vital information conduit to the entire research team.
• Maintain regular, proactive communication with study sponsors, CROs, and internal staff regarding study status, questions, and concerns.
• Collaborate with the Principal Investigator (PI) on the timely completion and submission of Serious Adverse Event (SAE) reports.
• Work closely with the data coordinator team for Case Report Form (CRF) completion and query resolution.

Study Oversight & Compliance :

Patient Management & Support :

Documentation & Training :

Administrative & Closeout :

Education and Experience :