Research Centers of America makes sure a solid data management plan is in place prior to study initiation.

We appreciate that accurate and efficient data exchange between the site and sponsors/CROs is critical.  Our staff’s extensive experience and knowledge, across a multitude of indications, contributes to our positive track record in both early and late phase trials. We pride ourselves in our level of data entry capabilities, averaging 24- to 48-hour turnaround times.  Similarly, the same attention is placed on query and safety resolution, as this is equally as important as initial database entry.

Our site enjoys building and maintaining relationships with sponsors and CROs.  To support our emphasis on confidentiality, we have a designated, quiet space for monitors to review and verify source data.  We work with monitors to schedule as many days as necessary to ensure all required data points are reviewed in a timely fashion.  Staff is available as needed to provide answers to any questions to ensure visits are as productive as possible.  Our goal is to aid in the success of research programs that translate into drug development and approval.

  • Dedicated, detail-oriented data entry staff
  • Source document review with CRF guidelines prior to study start
  • Accommodating to tight data entry timelines
  • Proficient with multiple EDC systems
  • Rapid query resolution in adherence with sponsor guidelines