Welcome to Prime Clinical Research
PCR – The Site with the right resources for excellent and efficient site management and monitoring. We are a multi-specialty clinical trial site endowed to perform clinical trial studies from phase1 to phase 4 with a diverse patient population.
About Prime Clinical Research Inc
PCR – Coordinates the most coherent and cost-effective clinical research trials through Sites, Healthcare partners, Homes and Telehealth to accelerate and optimize the process of getting you new medical product to the desired market in time to provide valuable solutions to life.
Our strength lies in our commitment to engaging a diverse range of patient populations, particularly focusing on the inclusion of minority communities. We value the representation of various cultural backgrounds, ethnicities, and socioeconomic groups.
How We Work
- Enable private practice physicians to bring research to their patients.
- Centralize administrative activities, reducing turnaround time.
- Intra-network referral system to bolster enrollment.
- The majority of our patients come from private practices in which they have close relationships with their doctors, which reduces number of patients lost to follow up and increases patient adherence to study schedules.
What we do?
- Patient Recruitment
- Study Procedure Administration
- Data Collection
- Safety Monitoring
- Compliance with Regulatory Standards
- Collaboration with Investigators and Sponsors
- IRB Coordination
- Community Engagement
- Quality Assurance
- General Study Management
WHY CHOOSE PRIME CLINICAL RESEARCH INC
Transforming Clinical Research Landscape
Our vibrant team of experienced Investigators, Research Nurses, Research Coordinators and site staff are appropriately selected and trained to conduct your studies following GCP and ICH guidelines as well as regulatory compliance requirements, ensuring you receive consistent feedback and support needed for high quality results. All staff are GCP and IATA certified with several years of clinical research experience.
Meet our Medical Team
Our team of Investigators are dedicated to excellence and committed to clinical study needs.
Tolulope Olabintan, MD, FAAFP, AAHIVS (Family Practice Physician)
Principal Investigator
Munira Dudhbhai, MD. PLLC (Obstetrician-Gynecologist)
Principal Investigator
Nepistance Shoko, MD (Internal Medicine)
Principal Investigator
Carola Okogbaa (Ophthalmologist)
Principal Investigator
State of the Art Facility
We have state of the art facility that provides all needed to run an unmatched trial.
• Waiting Area
• Multiple Patient Rooms
• Space for CRA/ Monitoring Staff
• 24-hour PK draws
• 21 CFR Part 11 compliant
• X-ray, FibroScan, PET, CT, sleep lab, DEXA within 5 miles
• 24 Hour Emergency Medical Center within 1 mile
Equipment
We have high quality equipments with industry standards. This equipments are well maintained and calibrated in compliance with regulatory compliance requirements.
• Medical Examination Tools- stethoscopes, thermometers, etc
• Laboratory Equipment - Refrigerated centrifuge, microscopes, and analytical instruments
• Patient Monitoring Devices - EKG machines, pulse oximeters, Blood pressure monitors
• Limited access drug storage
• Long term refrigerated, frozen, and ambient sample storage.
• Crash Cart
• 4C, -20C and -80C 24/7/365 temperature monitoring with backup power
• Data Management Systems – including Electronic Data Capture (EDC) platforms and secure data storage solutions for accurate and compliant data collection and management.
Qualified Staff
Our Investigators are all board certified physicians across multiple therapeutic areas including but not only: Internal Medicine, Family Medicine - Pediatrics, Dermatology, Ophthalmology, Endocrinology, Rheumatology, Nephrology, Gastroenterology, Cardiology, Pulmonology, Urology, Neurology, Gynecology, etcetera
Highest Quality Results
We provide reliable results and validate with pristine data.
Awarded Accolades
High customer satisfaction Sponsor Recognitions Happy Team
