Regional CRA Jobs in Illinois

Analyzing Information

Attention to Detail

Bioinformatics

Clinical Research

Authors/CoAuthors study protocols, develops study documents, identifies and enlists clinical sites, ensures availability of all clinical trial materials, facilitates IRB approval, trains investigators and their staff on the study procedures, oversees and monitors trials, maintains contact information, manages data and query resolution, ensures appropriate data analysis and writes the final report.

Collects information by searching and interviewing patients; comparing information discovered to information specifications; preparing correspondence.