Clinical Trials Management
HJF has extensive experience managing clinical trials in the military medical community, including Phase I–IV, single- and multi-site trials. Since our inception in 1983, we have supported more than 500 trials at most military medical centers and facilities. Our responsive and focused infrastructure enables you to accomplish your research goals quickly and cost-effectively.
Customers have access to our extensive research support services. In addition, our Clinical Trials Office provides personal assistance to help minimize administrative burdens.
Pre-Award Services
- Writing applications and IRB consent forms
- Negotiating and developing budgets
- Developing CRADAs and study agreements
- Compiling regulatory documentation
- Tracking protocols through IRB approval processes
- Acting as liaison with research sponsors
Post-Award Services
- Recruiting and hiring research support personnel
- Purchasing supplies and equipment
- Submitting protocol amendments
- Providing financial information
- Providing in-house travel services
Our staff is committed to quick turnaround times for IRBs to keep your proposal or project moving. When you work with HJF, you have a personal point of contact who is knowledgeable about your medical center and dedicated to your meeting needs.
HJF has a master CRADA with the Army and Air Force, reducing the approval processing time for the CRADA. Hence, only a Statement of Work (SOW) needs to be developed for new protocols at Army and Air Force facilities.
For more information, contact our Clinical Trials Office or alternatively, please contact our Office of Sponsored Programs. Researchers with current programs at HJF can access their detailed financial information through HJFOnline, our secure website. Detailed information on our services is available in our online Guide to Services.