Clinical Trial Manager

<h2 style="color:!important"><span style="color:#333333"><span><b><span style="font-size:inherit">Main Purpose of the Role</span></b></span></span></h2><ul><li><span style="color:#333333"><span><b><span style="font-size:inherit">Summarize the main purpose of the role</span></b></span></span><span><span style="font-size:inherit">Individual contributor with comprehensive knowledge in specific area.<br />Ability to execute highly complex or specialized projects.<br />Adapts precedent and may make significant departures from traditional approaches to develop solutions.</span></span></li></ul><h2 style="color:!important"><span style="color:#333333"><span><b><span style="font-size:inherit">Main Responsibilities</span></b></span></span></h2><ul><li><span style="color:#333333"><span><b><span style="font-size:inherit">List the main responsibilities this role regularly performs.</span></b></span></span><span><span style="font-size:inherit">Processes, reviews, and receives patient data and records and organizes clinical data forms from particular therapeutic groups and outside investigators.</span></span><span><span style="font-size:inherit">Provides accurate, timely, and consistent clinical data to the medical department and other groups.</span></span><span><span style="font-size:inherit">Responsible for data management plans including data preparation, data validation activities, etc.</span></span><span><span style="font-size:inherit">Follows Good Clinical Practices (GCP) data-handling procedures and guidelines.</span></span><span><span style="font-size:inherit">Requires knowledge of drug and disease terminology.</span></span><span><span style="font-size:inherit">May manage service providers that perform these activities.</span></span><span><span style="font-size:inherit">Participates in the review of clinical research protocols, reports and statistical analysis plans.</span></span></li></ul>