Exceptionally trained, regionally based Clinical Research Associates (CRAs) with an average of 10+ years clinical trial industry experience and over 1,000 site visits in the past three years.
KEY ADVANTAGES TO PARTNERING WITH PRC CLINICAL FOR CLINICAL SITE MONITORING:
PRC Clinical CRAs ensure that for every project, investigators are appropriately selected and trained to complete the study following GCP and ICH guidelines in order to produce high-quality study results.
Familiar with all EDC platforms
Our CRAs maintain a strong relationship with each study site, ensuring absolute quality and on-time receipt of all clinical trial deliverables.
Site focused CRAs that integrate with Sponsor teams and facilitate communication between sites and sponsors
Supported by ongoing trainings to remain current with industry content and trends
Developed and maintained full SOPs (Standard Operating Procedures)
PRC Clinical is the CRO of choice for many pharmaceutical, biotech and regenerative medicine developers worldwide, offering a next-level clinical trial management experience. Our innovative approach to executing studies merges our high-touch human element with high-tech tools, extensive experience and deep knowledge – far exceeding the level of service offered by large CROs. PRC Clinical offers full Clinical Trial Management services including Clinical Project Management, Site Monitoring, Quality Assurance, Drug Safety, Payment Services, Biostatistics, Data Management, Regulatory Strategies, and Site Selection.