Clinical Trial (Oncology)

The following lists contain items and processes that may be completed to ensure compliance with the rules and regulations that govern clinical research. The below fees will be charged to the study account established for the protocol and shall be covered by the organization that is sponsoring or funding the clinical research:

ProcedureDescriptionTotal
Administrative Start-Up A one time, non-refundable fee.$20,780
CTMS Set-UpA one-time, non-refundable fee$2,145
e-RegulatoryAn annual, non-refundable fee for CTU only$1,700
Administrative Annual FeeAn annual, non-refundable fee$6,530
Amendment FeeA non-refundable fee charged for each sponsor required IRB amendment and sponsor prompted budget or contract amendment. 

Regulatory$490
Financial $430
Pre-Screening FeeA non-refundable, quarterly fee, if applicableOutpatient$1,030
Inpatient $2,745
TrainingRequired additional protocol training for all personnel on DOA or 1572 through a sponsor system (per hour fee)Study Personnel$60
MD/PhD/PharmD$215
Sponsor/FDA AuditPer day fee
$615
Local SAE ReportingPer hour fee$85
IRB Initial ReviewA one-time fee$3,900
IRB Continuation ReviewAn annual fee$1,300
Administrative Close-OutA one-time, non-refundable fee$3,575
Archiving A one-time, non-refundable fee
$1,215

 

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