With more than 30 Principal Investigators representing a wide range of specialties, our sites offer unmatched depth and breadth of clinical expertise. This diversity allows us to support a broad spectrum of therapeutic areas, match the right investigators to the right studies, and ensure high-quality data collection. By leveraging this extensive PI network, we provide sponsors with the flexibility, efficiency, and scientific rigor needed to accelerate clinical development.

QCR Network accelerates the processes of feasibility, site selection, and negotiation internally, optimizing efficiencies for the Sponsor and CRO while ensuring high-quality, successful enrollment.

Accuracy matters. Our robust quality systems and meticulous data management practices guarantee reliable results that sponsors and regulators can trust. All QCR sites and studies are supported by in-house clinical data, quality assurance, regulatory, and risk management teams. The teams support all aspects of QA/QC processes to ensure adherence to all applicable FDA regulations, ICH GCP Guidance, state guidelines, industry standards, and QCR Network’s own stringent SOPs.

We have implemented a high-performing call center, with a minimum weekly call requirement. This ensures proactive engagement with stakeholders, streamlining communication, and facilitating seamless collaboration.

With patient acquisition costs as low as $3.30, our sites deliver unmatched efficiency in clinical trial recruitment and maximizing sponsors advertising budgets for their studies.

QCR Network has dedicated teams that actively engage with the community to ensure diverse representation in our patient recruitment efforts. Each of our sites customizes engagement strategies to reflect the unique cultural, linguistic, and health needs of the local population.

We engage in strategic partnerships with diverse organizations within our local communities to facilitate patient referrals to our studies.