First, fact management tools facilitate a central workspace for the trial team to collaborate on the key trial materials. (leandiscoveryblog.com)
• Provided logistical support in developing and writing clinical trial documents and manuals • Assisted in evaluating and investigative sites and conducting co-monitoring visits • Participated in monitoring study safety and handling data review and discrepancy resolution • Performed study initiation activities and reviewed protocols and regulatory issues • Documented accountability, stability and storage conditions of clinical trial materials according to sponsor's instructions (coverlettersandresume.com)
Work closely with process engineers for follow up and evaluation, and presented reports on trial materials according to designated schedules (resumegenius.com)