Access Whitepaper

First Name
Last Name
Thank you!
Error - something went wrong!

Shifting the Tide of Inefficient Site Contract Negotiations: Turn to an Expert

May 2, 2018

Working in the clinical research and drug development field is exciting and inspirational. Scientists, pharmaceutical companies, doctors and patients participate because of the promise it holds for humanity.

The tasks necessary to initiate sites so investigators can test a drug are numerous. For many, one such task, site contracting, is often considered mundane. However, because of the critical role a site contract plays in a clinical trial, it should be as inspirational as any other aspect.

Contracting may sound unexciting, but it’s just as important as IRB approval, patient enrollment— even the delivery of the medication to the site itself. No contract, no clinical trial.

Still, contracting should be dull—or at least uneventful. Too often, it’s stressful. It should be
a small part of activation process. Too often, it isn’t. It shouldn’t take so long or cost so much. Too often, it does.

Download this whitepaper to understand the elements of successful site contracting.

Previous Flipbook
Customized Scale Development
Customized Scale Development

We provided comprehensive training and quality control services, as well as one-on-one training in intervie...

Next Flipbook
In-Study Quality Control
In-Study Quality Control

We provided comprehensive training and quality control services on key efficacy measures and the appropriat...

Request a WCG Site Analytics report for your study

Get Site Intel