Is your study experiencing delays in enrollment or data entry due to staff shortages or gaps in your process? IMARC offers remote support and on-site research coordination to help keep your study moving forward. Our clinical research coordinator support helps you conquer data entry backlogs, complete enrollment, and resolve data discrepancies.
If you work at a site, you’ll have more time to enroll, consent and care for subjects. If you’re a study sponsor, you’ll have clean data sooner so you can get your study completed on time and your product to market faster.
Whether you need an extra set of hands screening participants or an extra set of eyes reviewing your data, our team can step in at any point. We can review electronic medical records remotely to extract and enter data on your behalf in the EDC. Here are a few of the ways we support your clinical research coordinator:
- Remote records review and data entry
- Data collection help on-site or remotely
- On-site assistance screening, enrollment, study procedures, or follow-up
- Prepare data for monitoring visits (on-site or remote) and achieve clean, completed CRFs sooner
IMARC provides comprehensive site support that starts with assessing your site and processes. Then our team will work as an extension of yours to develop solutions for more effective coordination and deliver results on time and on budget.