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Research Center Profile:
Crossroads Clinical Research, LLC

Center Information

Stacey Schendel
Research Director, Owner
Crossroads Clinical Research, LLC
1501 E. Red River Suite C-2
Victoria, TX 77901
USA
361-574-7800
361-574-7801 (fax)
sschendel@crossroadscr.net
www.crossroadsclinicalresearch.com
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Contact Center

Therapeutic Areas

Cardiology/Vascular Diseases
Dermatology
Endocrinology
Gastroenterology
Hematology
Immunology
Internal Medicine
Musculoskeletal
Nephrology
Neurology
Obstetrics/Gynecology (Women’s Health)
Oncology
Otolaryngology (Ear, Nose, Throat)
Pharmacology/Toxicology
Psychiatry/Psychology
Pulmonary/Respiratory Diseases
Rheumatology

Center Overview

Crossroads Clinical Research, LLC is a Multi-Speciality Research Organization which collaborates with multiple board certified investigators in a variety of therapeutic areas to conduct clinical trials within their practice. Crossroads Clinical Research, LLC works closely with the principal investigators to ensure that the clinical trials are conducted per the Code of Federal Regulations, Good Clinical Practices, and specific sponsor and protocol requirements. Crossroads Clinical Research, LLC was established in June 2011 by Stacey Schendel. Ms. Schendel worked as a Clinical Research Associate for two large Clinical Research Organizations for six years. Through her experience in monitoring multiple sites across the nation, she was able to gain the knowledge required to establish a superior site. The company began by cooperating with one principal investigator and has expanded over the past year to include five principal investigators in different therapeutic areas. 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.

Performance Metrics

Number of Studies Conducted: 20
Number of Studies Actually Completed: 5
Number of Active Patients in the Database: 55
Regulatory Submission Turn-Around Time: 10 Business Day(s)
Average Number of Total Patients Enrolled: 6
Average Percent of Total Patients Randomized: 65%
Average Percent of ‘Completed’ Studies that met Enrollment Goals: 100%
EDC Capabilities: Yes

Clinical Research Experience

Crossroads Clinical Research, LLC specializes in the following therapeutic areas:

  • Rheumatology
  • Internal Medicine
  • Nephrology
  • Obstetrics / Gynecology

Crossroads Clinical Research, LLC has worked with the following sponsors/CROs:

  • AstraZeneca
  • Merck
  • United Biosciences Coorporation
  • Eli Lilly
  • Chelsea Therapeutics, Inc.
  • Furiex Pharmaceuticals
  • Quintiles
  • Parexel
  • PPD
  • INC Research
  • Covance
  • PRA International

Facility Description

Crossroads Clinical Research, LLC works with investigators to conduct clinical trials in their own private practice setting. We have access to local imaging facilities such as x-ray and DXA scan, electrocardiogram machine, -20 freezer for storing frozen samples, blood draw stations, calibrated weight scales, calibrated centrifuge, and calibrated sphygmomanometer. We have an administrative office which includes a dedicated spacious area for chart review, high speed internet access (wireless and ethernet), storage area for study supplies, and study document storage. Our administrative office is located within one mile of our investigators private practice. We are located within 10 miles of the Victoria Regional Airport and have access to many name-brand hotels.

Investigator Experience


Noe R. Olvera, MD
Principal Investigator
Board Certified Rheumatology
Board Certified Internal Medicine
Five years of experience in clinical research


Richard H. Leggett, DO
Principal Investigator
Board Certified Internal Medicine
Two years of experience in clinical research

Haresh Kumar, MD
Principal Investigator
Board Certified Nephrologist
Board Certified Internal Medicine
One year of experience in clinical research

Faisal N. Khan, MD
Principal Investigator
Board Certified Nephrologist
Board Certified Internal Medicine
One year of experience in clinical research

Yvette F. Westford, MD, FACOG
Principal Investigator
Board Certified Obstetrician / Gynecologist
One year of experience in clinical research

Kathleen A. Parma, PA-C
Sub-Investigator
One year of experience in clinical research

Jean Gisler, FNP, PLLC
Sub-Investigator
One year of experience in clinical research

Staff Expertise

Stacey Schendel
Research Director, Study Coordinator, Owner
Six years of experience in clinical research


Dellene Clark, LVN
Study Coordinator
Four years of experience in clinical research

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.

Other Information

Crossroads Clinical Research, LLC uses a central IRB for all studies. We have worked with the following IRBs in the past:

  • Schulman IRB
  • Quorum IRB
  • Copurnicus Group IRB

Contact Center

If you are interested in contacting this center to discuss placing a clinical trial there, please complete and send the email form below. A representative from the research center will then follow up with you.

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