Sponsors and
Clinical Research Organizations (CROs)

Crossroads Clinical Research, LLC is dedicated to providing cutting-edge medical treatments to patients through clinical trials by collaborating with investigators to conduct clinical research protocols safely, ethically, efficiently, and accurately in order to produce quality data for sponsors.

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Patient Demographics

Our patient population is quite large as we are located in the "crossroads" of most major cities in Texas such as Houston, San Antonio, Austin, and Corpus Christi. We are the only clinical research operation in this area. There are many patients here who have never participated in a clinical trial, but are excited to have the opportunity without having to drive 200+ miles for study visits. We have a broad range of age, gender, race, ethnicity and financial standing among our patient population.

Facility Description

Crossroads Clinical Research, LLC works with investigators to conduct clinical trials in their own private practice setting. The following equipment is available:

>> Dedicated Research Exam Rooms
>> Imaging Facility including X-Ray, DEXA Scan and MRI
>> Temperature Controlled, Locked Study Drug Storage
>> Electrocardiogram Machine
>> -20 Freezer
>> Specimen Collection Stations
>> Weight Scales
>> Standard Centrifuge
>> Sphygmomanometer
All equipment is maintained and calibrated at least annually.

Administrative Office

We operate in an administrative office which includes a spacious dedicated area for source document review, high speed internet access (hard wire and wireless), copy/scan/fax machine, storage area for study supplies, and study document archiving. Our administrative office is located within five miles of our investigators private practice. We are located within 10 miles of the Victoria Regional Airport and have access to many name-brand hotels.

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Clinical Research Experience

Crossroads Clinical Research, LLC specializes in the following therapeutic areas:
Crossroads Clinical Research, LLC has worked with the following sponsors/CROs:
  • Amgen
  • Ardea Biosciences
  • AstraZeneca
  • Boehringer Ingelheim
  • Inventiv Health
  • Galapagos
  • Merck
  • United Biosciences Coorporation
  • Eli Lilly
  • Chelsea Therapeutics, Inc.
  • Furiex Pharmaceuticals
  • Quintiles
  • Parexel
  • PPD
  • INC Research
  • Covance
  • PRA International
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    Performance Metrics

    Number of Studies Conducted: 20
    Number of Studies Actually Completed: 9
    Regulatory Submission Turn-Around Time: 10 Business Day(s)
    Average Number of Total Patients Enrolled: 6
    Average Percent of Total Patients Randomized: 80%
    Average Percent of "Completed" Studies that met Enrollment Goals: 100%
    EDC Capabilities: Yes

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