Clinical Trial Monitoring
Clinical Trial Monitoring
ReachCatalyst Clinical Research Associates (CRAs) ensure the integrity of the study, adherence to protocol, quality of measurements, and safety of Subjects. We provide global monitoring and site management solutions to our clients via our international team of experienced professionals. ReachCatalyst CRAs have a minimum of five years' industry experience prior to joining our organization and are knowledgeable in all aspects of study conduct. CRAs are highly skilled, therapeutically aligned, centrally trained, and committed to excellence in every study.
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Furthermore, ReachCatalyst has developed a specialized CRA Training Academy as well as a Study Coordinator to CRA Bridging program, where we select talented professionals and cultivate their skills through an extensive training program on all facets of clinical research and trial oversight. This unique program allows us to introduce more individuals to clinical research careers and increases our pool of skilled CRAs to support clients' programs.
ReachCatalyst 's monitoring services include:
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On-site visits
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Remote visits, including remote review of source documents using established methods for secure file transfer
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Traditional 100% SDV or Risk-based Monitoring
Contract Research Organization (CRO)
ReachCatalyst is an award-winning Contract Research Organization (CRO) focused primarily in oncology, infectious disease, and CNS clinical research.
Patient Engagement Solutions
ReachCatalyst's full-service contact center improves patient recruitment, engagement and data collection through customizable, solution-oriented services.
Pharmacovigilance & Medical Information
ReachCatalyst's Pharmacovigilance group expertly manages clinical and postmarketing PV for drugs and devices, handling product safety, adverse events and reporting.