| Career description Clinical Research Coordinators (CRCs) help doctors improve the quality of clinical trial implementation and minimize their workload increase. The responsibilities of a CRC include arranging for a research study site, recruiting, screening and enrolling clinical study participants, arranging follow-up visits, maintaining and dispensing drug and other study supplies, completing and ensuring the accuracy of Case Report Forms (CRFs) and regulatory documents; and ensuring the adherence to Good Clinical Practice (GCP) guidelines. CRCs act like doctors' partners rather than assistants, and proactively give support throughout the process.
Despite importance, clinical trial implementation can be time-consuming and a considerable burden for doctors and staff in medical sites. CRCs help ensure that the clinical trials are performed seamlessly and minimize the stress placed on both the doctors and the patients.
Paula Bambino
Work: + 55 11 3068 0808 ext. 116/132
Fax: + 55 11 3085 7891
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