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Part-Time Clinical Research Coordinator
2 months ago
The Clinical Research Coordinator (CRC) will perform protocol specific duties relevant to the clinical trial in a defined scope that assists the site with patient recruitment.
Scope of Support:
- Administrative support customized site level support, such as support with regulatory document submissions and perform chart reviews/EMR interrogation
- Prescreening including review of concomitant medications, medical history, and inclusion/exclusion criteria to identify potential patients
- Scheduling patient visits including appointment reminders
- Data Entry and Query Resolution based on data available in source documents and ensure data entry and responses are completed within protocol designated windows
- External Referral Outreach including grassroots effort to distribute study recruitment materials in and around sites, community outreach
- Contact, screen, and schedule referrals from outreach campaign
- Conduct Study Visits
- Perform ICF process following GCP guidelines