Lead Clinical Research Associate
Current•Serving as Lead CRA on a project providing main contact for monitoring for the study, as well as development/maintenance of study monitoring plan. •Perform site qualification, initiation, routine monitoring, and close-out visits per ICH-GCP and other applicable SOPs and requirements.•Overall site management and main point of contact for assigned sites/studies.•Completion of visit reports and site follow-up letters.•Resource and training for new CRA’s