Clinical Research Coordinator I

Written By Miro Pastrnak

• Coordinates scheduling of patients for their studies (visits, physical therapy, MRIs, specialist appointments, follow-ups, etc.)

• Completes timely data entry, clearing of queries, and participant reimbursements

• Coordinates with Clinical Research Associate (CRA)/monitor for scheduling interim monitoring visits

• Documents notes to file (NTFs) and/or protocol deviations appropriately

• Orders and stocks study lab kits

• Sustains frequent and effective email communications between RDR and the CRO/Sponsor for questions and issues that may arise

• Communicates with potential new patients

• Makes and maintains organized subject binders

Miro Pastrnak
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