We connect innovation with patient care by conducting safe, ethical, and groundbreaking clinical trials that shape the future of healthcare
Why Partner With Berrey Clinical Research
We treat every participant with respect, compassion, and transparency.
Our team has extensive experience in clinical operations and regulatory compliance.
With strong community ties, we recruit diverse participants quickly and effectively.
Rigorous monitoring ensures data accuracy and reliability.
We work closely with sponsors, physicians, and participants for seamless execution.
From study start-up to patient follow-up, Berrey Clinical Research provides sponsors with end-to-end support. Our services include:
Leveraging strong community connections and outreach programs, we quickly enroll diverse participants while maintaining strict eligibility standards.
Our experienced team ensures all protocols meet FDA, IRB, and Good Clinical Practice (GCP) requirements, reducing risk and streamlining approvals.
With meticulous oversight, we capture accurate, reliable data that meets the highest industry standards for quality and integrity.
From site logistics to real-time updates, our team manages day-to-day trial operations and provides transparent reporting to keep sponsors fully informed.
When you volunteer for a study, you contribute to the development of new treatments that may improve health worldwide.
What you can expect:
Clear explanations and informed consent
Careful monitoring of your safety
Respect for your time and privacy
Possible access to new treatments at no cost
Our community outreach strategies and participant-centered approach ensure high enrollment rates, reducing delays and accelerating study startup.
We strictly follow FDA, GCP, and clinical best practices, ensuring every study meets the highest ethical and regulatory standards.
With electronic data capture and continuous monitoring, we deliver accurate, traceable, and reliable results for every protocol.
Our coordinators, investigators, and trained staff work together seamlessly to meet the unique needs of each clinical trial.
We maintain close collaboration with sponsors and CROs, providing regular updates and direct communication to ensure trust and alignment.
Our local presence allows us to engage with a wide range of populations, enhancing scientific validity and study impact.
Our community outreach strategies and participant-centered approach ensure high enrollment rates, reducing delays and accelerating study startup.
We strictly follow FDA, GCP, and clinical best practices, ensuring every study meets the highest ethical and regulatory standards.
With electronic data capture and continuous monitoring, we deliver accurate, traceable, and reliable results for every protocol.
Our coordinators, investigators, and trained staff work together seamlessly to meet the unique needs of each clinical trial.
We maintain close collaboration with sponsors and CROs, providing regular updates and direct communication to ensure trust and alignment.
Our local presence allows us to engage with a wide range of populations, enhancing scientific validity and study impact.
Without strong community strategies, participant enrollment can fall behind schedule, causing costly delays in study timelines.
Inexperienced teams may generate protocol deviations and compliance issues, putting the study at risk of audits or rejection.
Weak monitoring and manual processes increase the chance of errors in data collection, compromising study outcomes.
Without specialized staff, trials face higher risks of non-compliance, extended timelines, and unexpected costs.
Lack of clear and frequent updates can lead to misunderstandings and misalignment between sponsors, CROs, and research sites.
Without targeted outreach, studies often end up with homogeneous populations, reducing both the validity and applicability of the results.
