Clinical Research Associate working on global projects in healthcare. Focused on site monitoring, recruitment plans, and protocol training with dedicated mentoring.
Responsibilities
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Supporting the development of a subject recruitment plan
Establishing regular lines of communication plus administering protocol and related study training to assigned sites
Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Requirements
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience
2 years of clinical research coordinator experience strongly preferred
Alternatively, an equivalent combination of education, training and experience
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