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 Next Level in Clinical Trial Management. Since 2003, we have specialized in providing pharma/biotech, and medical device sponsors, with clinical project management, feasibility and site selection to meet on-time enrollment goals, site management and monitoring and eTMF trial document management services, as well as a host of online management tools that streamline metrics reporting and unify the study team. PRC Clinical offers a range of other clinical trial services as well, including Data, Safety, Laboratory, and consultation services through a network of long-established strategic support partnerships.