Our Investigator Team
-Medical Director and Principal Investigators provide clinical oversight in all daily clinical trial activities.
-We don’t waste time. A lot goes into starting up a new study, and every partner has to do their part. As soon as we are awarded a trial, we initiate startup activities including contract negotiations, regulatory submission, and study team training.
-IRB Regulatory submission is fast and organized. Single point of contact is the same from startup to closeout.
Optimized Patient Recruitment
-Recruitment begins with IRB approval and doesn’t stop until your study is completed
Operations and Quality
-Lead coordinator, backup coordinator, & team assignments based on experience.
-Administrative & patient recruitment duties shared across administrative support team.
-Single Point of Contact for your team from start-up through completion.
Facility and Equipment
-Our Facility is located in Austin, TX at the intersection of 3 major highways, 2.2 miles from a hospital, and less than 10 miles to Austin Bergstrom-International Airport.
You can expect to find plenty of exam rooms, dedicated monitor’s offices, state of the industry technology, ample space for regulatory files, calibrated diagnostic equipment, as well as a CLIA waived laboratory, freezers, refrigerators, and a secured, temperature-monitored drug storage room.