Responsibilities and qualification of CMX Clinical Research Coordinator

Contact Roger Sharpe
to discuss your research project at
416.435.1746 or rsharpe@cmxres.com.

Responsibilities and Qualifications of a CMX Clinical Research Coordinator

CMX Research Inc. provides highly trained and experienced CRCs to maintain workflow at investigative sites.

CRCs participate in site selection, qualification, initiation, interim monitoring and close-out visits. They carry out protocol activities and complete documentation such as charting, data entry (EDC) and drug accountability records. In addition, CRCs follow-up with study participants and manage study duties as assigned by the principal investigator.

Flexible Schedules

Our CRCs can be hired on an occasional basis, part time or at full time hours to fulfill the study obligations. CRCs are CMX Research Inc. employees and therefore we take responsibility for the quality of their work.

Minimum Qualifications for CRCs at CMX Research Inc.

Bachelor of Science Degree in a health related discipline
Nursing degree is preferred
Minimum 2 years experience as a CRC
Comprehensive knowledge of GCP/ICH and other applicable regulatory guidelines
Sound understanding of clinical research process
Excellent organizational and problem solving skills
Outstanding verbal and written communication
Computer literate in MS software
Certified, or attending certification program at a recognized institution

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Responsibilities and Qualifications of a CMX Clinical Research Coordinator