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:

Procedure Description Total
Administrative Start-Up  A one time, non-refundable fee. $20,780
CTMS Set-Up A one-time, non-refundable fee $2,145
e-Regulatory An Initial fee at start-up and annually thereafter, non-refundable $1,700
Administrative Annual Fee An annual, non-refundable fee $6,530
Amendment Fee A non-refundable fee charged for each sponsor required IRB amendment and sponsor prompted budget or contract amendment. 

Regulatory $490
Financial $430
Pre-Screening Fee A non-refundable, quarterly fee, if applicable Outpatient $1,030
Inpatient $2,745
Training Required 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 Audit Per day fee
$615
Local SAE Reporting Per hour fee $85
IRB Initial Review A one-time fee $3,900
IRB Continuation Review An annual fee $1,300
Administrative Close-Out A one-time, non-refundable fee $3,575
Archiving  A one-time, non-refundable fee
$1,215

 

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