Align yourself with the premier clinical research site network, dedicated to discovery and diversity. Featuring centralized management, highly coordinated recruiting and a multi-skilled medical staff, Alliance Clinical Network is recognized as an industry innovator.
Why Our Network Works…
Extraordinary forethought has gone into the establishment and growth of Alliance Clinical Network. Our closely-managed group of research sites extends across Texas, California and Nevada. Primarily located on local hospital campuses or within close proximity, the sites benefit from a centralized, hands-on management approach for consistency and strong oversight. We recruit volunteers from a largely minority patient population, tapping into a vastly underserved, highly crucial research base.
The Alliance management team works closely with CRO’s and Sponsors desiring an efficient, well-coordinated network that consistently meets enrollment goals, builds high quality staffs and maintains steady profitability. Our large, qualified patient database, 24/7 business model and decades of research experience across numerous therapeutic areas have made us a recognized industry leader.
People and Technology
Combining experienced, dedicated health professionals and the latest medical and management technology, the Alliance Clinical Network has built a solid reputation for dependable excellence. We leverage our capabilities to ensure consistent study execution, quality controls, and easy scalability.
Here are just a few of our network strengths:
- Streamlined site management for greater efficiency
- Strong relationships with blue-chip sponsors and CRO’s
- Technology and processes that standardize operating procedures across all sites
- Database containing well over 100,000 patients
- Lab testing and special services that foster patient engagement
- Secure on-site pharmacies with licensed pharmacists
- State-of-the-art e-clinical technology for sourcing, scheduling, patient interaction, records management and more
With a Wide, Clear Focus
We excel in many different areas of therapeutic study, including:
- General Medicine
- Infectious Diseases
- Internal Medicine
- Women’s Health
We have perfected this model so that we can effectively activate a site, including seeing our first patient, within 35 days of the site inspection visit.
A robust patient database, with mechanisms to identify patients by age, gender, medical history and more, enables us to engage target volunteers within minutes and secure their participation.
With skilled in-house clinical research associates and a 24/7 business that runs continuously, we can conduct study oversight that is efficient and thorough. Our ability to address and complete all quality control queries ensures Good Clinical Practice (GCP) compliance and smooth execution of all trials.
Proficiency in site activation time, patient volume and quality control generates cost savings that we pass along to our sponsors. By maintaining a high level of quality, fewer site issues need to be remediated, trials move more quickly and vital drugs make it to market faster.