This form seems complicated. Shouldnt the Office of Clinical Trial Operations be responsible for completing this information?
No. While the OCT is available for support to help complete the billing plan, it is the obligation of the PI to assume full responsibility for appropriate planning and assessment related to the specifics of the clinical research project and to be able to communicate that information to the institution. The PI and research team should be fully aware of all procedures/tests/visits/ and test articles associate with the project and be able to communicate those accurately through the use of the billing plan.
