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Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

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Page 1: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Budget DevelopmentPresented by:Jean Mercer

Associate Director for Clinical Research Administration

Office of Clinical Research – School of Medicine

Page 2: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Topics that will be covered

Systems for budget development. Identifying items to budget. Standard of care items. Identifying pricing information.

Page 3: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

More Topics

Indirect costs Start up expenses Screen failures Budget feasibility

Page 4: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Systems for Budget Development

Study Manager Contact Karen Best (8-5850) for

training

Excel Spreadsheet

Page 5: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

How do I identify what items I need to budget?

Review the Schedule of Activities spreadsheet in the protocol.

Review the Study Procedures section of the protocol.

Page 6: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Identifying Items to Budget

Review the budget exhibit or section of the contract agreement.

Talk with the Research Coordinator (if applicable) who will be involved with the study.

Page 7: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

What about Standard of Care Items?

As you review the protocol look to see what tests and procedures may be considered Standard of Care for the patient population involved in the study.

Identify these items as SOC on your budget spreadsheet.

Page 8: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

How do I find the cost information for procedures/tests?

Contact the appropriate area to obtain pricing information. (See contact list)

Use Study Manager to obtain pricing information for Clarian procedures.

Page 9: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Indirect Costs Do I really have to include these? (Yes )

The current indirect cost rate for an industrially sponsored clinical research trial is 25%.

The current indirect cost rate for a federally sponsored clinical trial is 33.5%.

Page 10: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Commonly Requested Start Up Costs

IRB Fee - $2,000 (only if industrially sponsored)

IRB Submission Effort – average is $1,500 - $2,000

Pharmacy Set Up Fee – determined by Investigational Pharmacy.

Page 11: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Commonly Requested Start Up Costs (cont.)

Administrative Start Up Fee – average is $2,000

Archival/Storage Fee – storage of records after study has been completed. Average budget is $750.

Close out/Queries for Data Lock – Average budget $750 - $1,000.

Page 12: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Additional Start Up Fees Effort for nurse coordinator and PI

to attend study start-up meeting hosted by sponsor.

Effort involved for FDA Audit.

Page 13: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Non-Refundable Costs IRB Fee IRB Submission Effort Pharmacy Set Up Fee Administrative Start Up Fee

Even if a study does not enroll any patients you need these basic costs covered.

Page 14: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Screen Failures Goal is to get at least the cost for the

first visit covered if a patient does not pass the screening process.

Many Sponsors want to pay a minimal amount for screen failures.

Evaluate your study to determine if you expect to have several patients drop out. Negotiate with the sponsor on this number.

Page 15: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Budget Feasibility

Is it feasible to conduct this trial with the current budget from the Sponsor?

If it is not feasible, then what is the bottom line amount you must have?

Page 16: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Negotiating the Budget Find out who the contact is at the

pharmaceutical company that you should work with.

Send an email or call the contact person and introduce yourself.

Send via email your detailed spreadsheet with the proposed IU budget and ask the Sponsor to review it.

Page 17: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Internal Budget

IU requires that a brief internal budget be included when you route your contract.

Example:Direct Costs $25,000

Indirect Costs 6,250 (25% IC rate) IRB Fee 2,000

Total Costs $33,250

Page 18: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

Routing of the Contract You can route your contract while

the budget is being negotiated. Just note on the route sheet that the

budget is not finalized yet.

It is preferred that you use an ERA route sheet and attach the electronic files for the internal budget and contract.

Page 19: Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine

QUESTIONS?

Contact Jean Mercer Phone: 278-5843 Email: [email protected]