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FIND A TRIAL NEAR YOU

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A Partner to Research Professionals

The Accel Research Sites Network offers leading sponsors, clinical research organizations, and healthcare providers the ability to execute multi-phase clinical research studies. With a focus on precision and speed, our facilities are built for flexible, results-focused studies, able to be set up and executed on limited timelines. With decades of experience in the healthcare innovation space, you’ll trust that every study, every patient, and every outcome will be meticulously managed – with evidence-based results.

7

Clinical Research Units

16

Embedded Research Sites

260k+

Diverse Patient Database

Phase I-IV Clinical and Device Capabilities

30+

Experienced Investigators

204

Different Indications in 30+ Therapeutic Areas

  • Recruitment

    Our internal database of over 260,000 patients, dozens of disease-specific social communities, in-house call center, and expert eligibility review are all at your disposal when you partner with Accel. Our partners in large medical practices can also identify and educate potential research subjects for your study, while we develop a custom marketing plan and creative for every study to attract participants.

  • Study Performance

    From pre-selection and start-up, to study conduct and closeout, each trial is supported by a full-time director and coordinator. Our team monitors 100 data elements related to each trial across its entire lifecycle and are experts in source document creation and training facilitation.

  • Regulatory Affairs

    Our Regulatory Affairs team prides itself on rapid processing of regulatory packets and the utmost attention to detail. Your study’s regulatory documents will be hosted in an industry-leading site regulatory platform, where your study team will have immediate on-demand access to the documents it needs from anywhere in the world.

  • Fast Start-Up Times

    We understand time is key when it comes to bringing new healthcare innovations to market. At Accel, we can start studies quickly as we are not subject to long internal review processes or internal IRBs. Our target start-up timetime, including regulatory affairs and contract execution, is 10 business days or less.

  • Quality Control & Compliance

    Our research coordinators are dedicated, full-time professionals with valuable industry experience. In addition to required certifications such as GCP and IATA, they undergo regular general and study-specific training to ensure total compliance with study requirements while maintaining patient safety and data integrity. With little coordinator turnover, we provide a consistent experience for the study team and patients alike. Our Quality Control team reviews all documentation to ensure the highest quality data, and Internal Quality Assurance and Monitoring from independent experts supports our constant commitment to quality and compliance.

  • Laboratory

    All of our dedicated clinical laboratory staff are IATA certified and trained to process a wide range of samples. They are familiar with time-sensitive processing such as PK and antibody processing, sputum samples, flash freezing, 24-hour urine collection, rapid antigen, and PCR via nasal swabs or washes. We use high-quality, scientific laboratory-grade equipment that is professionally maintained and calibrated.

  • Investigator Oversight

    Each of our Investigators are respected members of the medical community with a true scientific interest in their studies. We are a clinical organization first, engaged in meaningful development work that delivers new treatment options to patients, and our Investigators are proud to wear the Accel Research Sites Network name. It is with this same pride and enthusiasm that these full-time providers will devote themselves to your study and its subjects.

Are you interested in joining our research network?