Expand your practice and bring cutting-edge clinical research to your patients with full support from our experienced team. We help physicians new to research to set up and run compliant studies from IRB submissions, GCP training, and site start up to patient recruitment and coordination - so you can offer innovative treatments, enhance your professional profile, and add a new revenue stream.
Our strong study pipeline management keeps your site active and profitable by tracking new trial opportunities, completing feasibilities quickly, and planning resources early. This proactive approach reduces start-up delays, avoids revenue gaps, and ensures a steady flow of high-value studies that match your patient population.
Our team provides full administrative support to keep your site running smoothly from budget and contract negotiation and quick study start ups to invoicing and financial management. We also handle eSource creation, eReg/eSource quality assurance, and ensure your site is compliant and study ready with minimal burden on your staff.
Boost your enrollment with our comprehensive patient recruitment support, including community outreach, onsite or remote chart reviews, patient contacting and medical records retrieval, and targeted local social media campaigns. We help fill your trials faster by connecting the right patients to the right studies while reducing the worklo
Boost your enrollment with our comprehensive patient recruitment support, including community outreach, onsite or remote chart reviews, patient contacting and medical records retrieval, and targeted local social media campaigns. We help fill your trials faster by connecting the right patients to the right studies while reducing the workload on your site. We keep patients engaged through personalized follow ups.
We offer electronic source (eSource) and electronic regulatory (eReg) binder setup and management, streamlining data capture and document control. These tools reduce errors, speed up monitoring and audits, ensure compliance, and help your site launch and run studies more efficiently.
We provide full financial management support including clinical trial agreement (CTA) and budget negotiation, timely invoicing, and tracking and collection of payments to ensure your site gets paid accurately and on time while maximizing study profitability.