Innovation in Investigator Site Contracting

June 11, 2018

In the perpetual pursuit of a more efficient clinical research process, biopharmaceutical sponsors and contract research organizations (CROs) have traditionally focused their resources on the more costly and time-consuming aspects of study start-up such as protocol development, regulatory and ethical review, and data management and analysis. Investigator site contracting and management of site payments are often overlooked as opportunities to accelerate study start-up and to reduce the expense and complications of managing study site contractual relationships.

However, by targeting this smaller, yet still significant, aspect of study start-up, sponsors and CROs can expedite the process of contract negotiation, reducing both the cycle time and burden on the legal infrastructure.  

Download this whitepaper to learn more.

Previous Video
Speed, Efficiency and Accuracy in Site Contracts and Payments
Speed, Efficiency and Accuracy in Site Contracts and Payments

Learn how sponsors and CROs can optimize site contracting and payments management to expedite the process o...

Next Flipbook
Case Study: Initiating Sites Faster Through Efficient Contracts and Payments
Case Study: Initiating Sites Faster Through Efficient Contracts and Payments