Celena Cousins

About Celena Cousins

I\'ve worked as a Clinical Research Coordinator for 5 years and I\'m well experienced. I…

Experience

1. Central Study Coordinator Dct

   Care Access

   Jul 2022 — Present

   Interpreted protocols and advised treating physicians on appropriate dosage modifications and treatment calculations based on patient characteristics. Prepared study related protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports. Assessed eligibility of potential subjects through methods such as screening interviews, reviews of medical records and discussions with physicians and nurses. Identified protocol problems, inform investigators of problems and assist in problem resolution efforts, such as protocol revisions. Collaborated with investigators to prepare presentations and reports of clinical study procedures, results and conclusions. Proposed study protocols to evaluate factors such as sample collection processes, data management plans and potential subject risks. Maintained contact with sponsors to schedule and coordinate site visits and to answer questions about issues such as incomplete data. Maintained required records of study activity including case report forms, drug dispensation records and regulatory forms. Recorded adverse event and side effect data and conferred with investigators regarding reporting of events to oversight agencies.