Clinical Trials W or kshop. Presenters: Thomas Landis, Senior Grants and Contracts Officer Erika Waday , Information and Training Specialist Jennifer Bingham, Grants and Projects Analyst II. Clinical Trials Process Overview. Contemplating a Clinical Trial .
Thomas Landis, Senior Grants and Contracts Officer
Erika Waday, Information and Training Specialist
Jennifer Bingham, Grants and Projects Analyst II
Role of OSP: To negotiate terms and conditions of the agreement to ensure NSHE policies and procedures are adhered to and NSHE and study team are protected.
Role of PI and Study Coordinators: Negotiate budget, initiate request for IRB approval to generate ICF, provide input and approval as to CTA terms to OSP and coordinate with OSP in transmitting CTA “package” to sponsor.
When payment is based upon case report forms, you (the site) will bill the sponsor directly for patient visits. If payments can’t be submitted by case report, OSP will bill on your behalf.
Examples of costs for which most sponsors need to be directly billed:
Board of Regents
Attn: Controller’s Office/Cashier
1664 N Virginia Street Mail Stop #124
Reno, NV 89557