Embedded Files
Who does what?
Who does what?
What CTO services require funding, and what services are provided by MCC?
What are the roles and responsibilities of the research team? (NCI webinar slides)
Team roles and responsibilities for a la carte services (in development)
Resources available at the Clinical Research Support Center (CRSC @ CTSI)
What tasks can be delegated? (click to expand)
What tasks can be delegated? (click to expand)
A. Determine subject eligibility: Sub-I
B. Obtain subject informed consent: Sub-I, CRC-RN, Treating Physician
C. Perform Physical Exam: Sub-I, Treating Physician, APP
D. Perform Drug Accountability: IDS, CRC-RN, CRC
E. Prepare and dispense study drug: IDS
F. Instruct subject on study drug administration: CRC-RN, Sub-I, Treating Physician, APP
G. Disease assessment evaluation: Sub-I, Treating Physician
H. AE/SAE attributions: Sub-I
I. Safety/deviation reporting: CRC-RN, CRC, RS
J. CRF completion/query resolution: CRC-RN, CRC
K. Provide regulatory support: RS
L. Handle/ship research laboratory samples: CRC
M. Signing treatment plans: Sub-I, APP (non-CTEP studies), Treating Physician
N. Initial Protocol Training: Sub-I, CRC-RN, CRC, PM
O. Other (specify, if applicable)
Ancillary Review Process
Ancillary Review Process
Additional Services and Training
Additional Services and Training
Training on Grand Avenue (Document library and training for all CTO Work Instructions, SOPs, Forms, Tools, and Policies)
Page updated
Report abuse