Clinical Research Professionals, LLC

Center Information

Candace Grasse
COO/Owner
Clinical Research Professionals, LLC
#7 The Pines Court Suite D
St. Louis, MO 63141
USA
636-220-1200
314-667-3331 (fax)
cgrasse@clinicalresearchprofessionals.net
www.clinicalresearchprofessionals.net
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Currently Enrolling Trials

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Therapeutic Areas

Cardiology/Vascular Diseases
Dental and Oral Health
Devices
Endocrinology
Family Medicine
Gastroenterology
Genetic Disease
Healthy Volunteers
Hematology
Hepatology (Liver, Pancreatic, Gall Bladder)
Immunology
Infections and Infectious Diseases
Internal Medicine
Musculoskeletal
Nephrology
Neurology
Nutrition and Weight Loss
Obstetrics/Gynecology (Women’s Health)
Orthopedics/Orthopedic Surgery
Otolaryngology (Ear, Nose, Throat)
Plastic Surgery
Psychiatry/Psychology
Pulmonary/Respiratory Diseases
Rheumatology
Sleep
Urology
Vaccines

Center Overview

Our Mission
WE ARE DEDICATED TO MANAGING CLINICAL RESEARCH TRIALS WITH INTEGRITY AND PROFESSIONALISM.

Clinical Research Professionals (CRP) is a privately owned dedicated research company that provides a network of physicians who work collaboratively in conducting clinical research trials. We have multiple offices throughout the St. Louis, Missouri metropolitan area. Our volunteer participant database is extensive with over 35,000 people.

Our team consists of certified research professionals helping to improve lives through the advancement of new drug therapies and medical devices. With over 22 years of clinical trial research experience, we partner with physicians and sponsors to participate in clinical research trials. Our high quality services can be customized to meet the individual needs of the clinical trial and the site.

We provide all the necessary resources, including research staff and equipment in the physician’s office to maximize compliance and convenience. By providing these services in the physician’s office, physician oversight and availability is enhanced, medical records remain on site for immediate access and to assure confidentiality, and patient and physician confidence levels are maximized. Our physician medical partners are certified in multiple therapeutic areas and have over 20 years of medical clinical experience. Additionally, we have an expanded network of over 60 physicians who work collaboratively to meet enrollment goals.

We specialize in complex study oversight and organization in all trials and we provide the infrastructure and the trained and skilled personnel to manage specialized trials. We provide seasoned professionals with therapeutic and operational experience in Regulatory, Recruitment, Budgets/Contracts and Coordination. Our Clinical Coordinators are certified and have degrees in a variety of medical areas, including nursing and respiratory therapy. The average years of clinical trial experience for each member of our team is over 10 years. All CRP employees are extensively trained in GCP and research, as well as patient care, in order to elevate site performance and enhance the patient’s experience. Our SOP’s are thorough and specific to the clinical research industry. We are dedicated to the highest quality clinical trials and are committed to providing integrity within our team and in our data. Our physicians have documented extensive, thorough training.

We look forward to an opportunity to work with you and your team to help you achieve your objectives and exceed your goals.

Performance Metrics

Number of Studies Conducted: 150+
Number of Studies Actually Completed: 150+
Number of Active Patients in the Database: 35,000+
Regulatory Submission Turn-Around Time: 5 Business Day(s)
Average Percent of ‘Completed’ Studies that met Enrollment Goals: 98%
EDC Capabilities: Yes

Clinical Research Experience

Our experience includes phases 2-4 in the following therapeutic areas:

  • Migraine Headaches
  • Insomnia
  • Alzheimer's Disease
  • Memory Impairment
  • Restless Leg Syndrome
  • General Anxiety Disorder
  • Depression
  • Hyperlipidemia
  • Hypertension
  • Coronary Artery Disease
  • Heart Failure
  • Diabetes - Type I & II
  • Obesity
  • Osteoarthritis
  • Pain
  • Male Sexual Dysfunction
  • Female Sexual Dysfunction
  • Overactive Bladder
  • Heartburn
  • IBS
  • Nocturia
  • Vaccines
  • Parkinson's Disease
  • Tendinitis
  • Low Back Pain
  • Ulcerative Colitis
  • Crohn’s Disease
  • Colonoscopy Studies
  • Psoriatic Arthritis
  • Lupus
  • Rheumatology
  • Traumatic Brain Injury

Services

  • Clinical Trial Identification
  • Site/Physician Profile Creation
  • Study Start Up (including naive sites)
  • SOP Creation (research specific)
  • Training
  • Audit Support
  • Regulatory Filing
  • Budgeting
  • Organization and Support
  • Safety Monitoring
  • Data/Clinical Record Monitoring
  • Archiving Services
  • Data Analysis
  • Employee Recruitment and Training
  • Study Enrollment
  • Physician Recruitment
  • Subject Recruitment
  • Subject Database Building

Facility Description

Clinical Research Professionals (CRP) provides all of the necessary resources, including research staff and equipment in the physician’s office for clinical research trials. By providing these services in the physician's office, physician oversight and availability is enhanced, medical records remain on site for immediate access and to assure confidentiality. Compliance and convenience are maximized. We specialize in complex study oversight and organization by providing the infrastructure and the trained and skilled personnel to manage the unique needs of each trial.

Investigator Experience

Our physician medical partners are certified in multiple therapeutic areas and have over 20 years of medical clinical experience. Additionally, we have an expanded network of over 60 physicians who work collaboratively to meet enrollment goals.

Staff Expertise

Clinical Research Professionals (CRP) provides seasoned professionals with therapeutic and operational experience in Regulatory, Recruitment, Budgets/Contracts and Coordination. Our Clinical Coordinators are certified and have degrees in a variety of medical areas, including nursing and respiratory therapy. The average years of clinical trial experience for each member of our team is over 10 years. All CRP employees are extensively trained in GCP and research, as well as patient care, in order to elevate site performance and enhance the patient's experience. Our SOP’s are thorough and specific to the clinical research industry.

Patient Demographics

St. Louis Demographics:

Metro Population 2,856,000
Race - 76.9% white, 18% black, 2.1% Asian, 1.1% Other race, 2.5% Hispanic/Latino
Gender - 48.4% male, 52.6% female
Colleges/Universities - 209,000 enrolled in 40 colleges

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.