SPONSOR/ CRO INFORMATION

Thank you for your interest in our dedicated clinical research and vaccine center, Clinical Research Professionals.  We are dedicated to the ethical and professional management of clinical trials, with integrity and quality being a leading value.  Our team members are trained medically and hold multiple certifications.  Clinical Research Professionals has dedicated and experienced specialists for regulatory, recruitment, budgets and contracts in addition to our clinical team.  A regulatory submission can be completed in as little as 3 days.  Our average contract and budget timeline is 7-10 days.  Our dedicated recruitment department assures successful enrollment of appropriate study participants.  We are committed to excellence.

Please click this button to fill out the contact request form and one of our clinical research professionals team members will contact you. We look forward to working with you for all of  your research needs.

SERVICES
Please visit our services page for more information


Clinical Trial Management
Employee Training
Employee Mentoring
Safety Monitoring
Archiving Services
Data Analysis


Monitoring
SOP Creation
Audit Support
Regulatory Filing
Budgeting
EXPERIENCE
Our experience includes phases 2-4 in the following therapeutic areas
Migraine Headaches
Alzheimer’s Disease
Memory Impairment
Restless Leg Syndrome
General Anxiety Disorder
Depression
Gastroparesis
EoE (Eosinophillic Esophagitis)
Hyperlipidemia
Hypertension
Coronary Artery Disease
Diabetes – Type I & II
Obesity
Osteoarthritis
Pain
Male Sexual Dysfunction
Female Sexual Dysfunction
Overactive Bladder
Heartburn
IBS
NASH
Nocturia
Ulcerative Colitis
​Traumatic Brain Injury
Vaccines
Parkinson's Disease
We look forward to an opportunity to work with you and your team to help you achieve your objectives and exceed your goals.
To View Our Clinical Trial Experience Click Here