Our monitoring group consists of CRAs with greater than 10-years of all-phase Pharma, Device and Biotechnology trial experience. There are no “box-checkers” here. Our CRAs are engaged professionals with superb problem-solving skills, adept at the most complex of clinical studies. Their values align with the core culture at Research Echo: dedication, precision and integrity and we’re thrilled to have them part of our team. Monitoring tasks include Site Evaluation Visits, Site Initiation Visits, Interim Monitoring Visits, Close-out Visits, Risk-based Monitoring and Rescue.

Our monitoring group consists of CRAs with greater than 10-years of all-phase Pharma, Device and Biotechnology trial experience.  There are no “box-checkers” here. Our CRAs are engaged professionals with superb problem-solving skills, adept at the most complex of clinical studies. Their values align with the core culture at Research Echo: dedication, precision and integrity and we are thrilled to have them part of our team. Monitoring tasks include Site Evaluation Visits, Site Initiation Visits, Interim Monitoring Visits, Close-out Visits, Risk-based Monitoring and Rescue.

The deliverable of any clinical trial is always unique; and to reach that endpoint on time and with success requires a specific skillset and sensibility of the individual in charge of this monumental task. Communication is critical, as is proper pre-execution planning, patience, ongoing team guidance, observation and re-evaluation to identify any crucial issue that may threaten a project’s quality or timelines. How we’re different here? Our PMs believe that leadership is about action – they don’t just talk, they do.