Clinical Research Associate
Current- Feasibility Management;- Translations review; - Conduction of qualification, initiation, monitoring, and closeout visits;- Communication with the medical site staff;- Verification of adequate investigator qualifications, training, and resources;- Review and Verification of Source documents and data;- Review of medical device and/or investigational product/drug accountability and inventory;- Review and Verification of patient safety data and its timely reporting;- Support sites with their patient enrollment and retention challenges;- Completion of monitoring reports and follow-up letters;