Clinical Research Coordinator

Under direction of the Senior Manager of Clinical Trial Operations, the Clinical Research Coordinator II, CTO (CRC II) manages and conducts the day‑to‑day activities of a research study. In general, the CRC II ensures the study maintains accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements. Beyond administrative duties, responsibilities of a CRC II may include subject recruitment (screening, consenting support and enrollment), follow‑up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CROs and regulatory authorities.

• Attends and participates in investigator meetings, pre‑study visits, and initiation meetings or coordinator meetings as appropriate.
• Collects and maintains accurate patient data for submission to sponsor, maintaining proper patient records, coordinating the collection, and shipments of specimens as required by protocol.
• Communicates study objectives/procedures to relevant hospital units involved with the study including the establishment of good rapport with the Principal Investigator and providing required assistance.
• Communicates with the sponsor or their representatives, schedules and facilitates study monitor visits, and facilitates communication between Principal Investigator and sponsor or sponsor’s representatives.
• Complies with the Research Finance Compliance policies and procedures including reporting requirements to research finance staff.
• Interacts with patients and families to recruit (screen, consent and enroll) study subjects and ensures compliance with the protocol.
• Responsible for speedy and adequate patient enrollment as determined by Research Management and Principal Investigator in all assigned studies.
• Submits new protocols to Research Regulatory Affairs team (for IRB submission/approval) and verifies proper documents were received with the proper format.
• Demonstrates and utilizes Good Clinical Practices in the conduct of clinical trials as per established protocol.
• Follows NCRI Standard Operating Procedures, AAHRPP, HIPAA, and FDA guidelines for clinical research, and keeps updated in those procedures and/or guidelines.
• Enters required data into CTMS.
• Provides new protocols, amendments, and study status updates to necessary research staff for digitization/entry into CTMS.
• Works adjusted hours to accommodate subject visits.
• Keeps electronic patient files and required documents up‑to‑date within e‑regulatory system.

The ideal candidate has experience with Hematology/Oncology.

• Bachelor’s degree and 2 years of research experience (OR irradiant) Associate’s degree and 4 years of research experience
• (OR) 5 years of research experience

• Experience in pediatric clinical research in a hospital setting.
• Clinical research certification (CCRC, CCRP, CRA) and IATA certification preferred.
• Experience working on clinical trials, interventional studies is preferred.
• Excellent communication skills in working with both children and adults.
• Excellent organizational skills, detail‑oriented, people‑oriented, flexible, and adaptable to change.
• Knowledge of protocols and its process.
• Experience with software applications including word processing, scheduling and contact database, email, web browsing, hospital records, other database software and office equipment.
• өйСтандарт relevant hospital equipment for each clinical trial project.
• Availability to work adjusted hours to accommodate subject visits.

Mid‑Senior level

Full‑time

Health Care Provider