<p>Department</p> <p>Women's Cancer Care Grant</p> <p>Job Summary</p> <p>Prepares and submits regulatory submission to IRB and sponsors, documentation compliance for multiple study projects, audit preparation, and data submission. This position also will be responsible for advising patients of trial design, facilitating informed consent for investigators, following strict adherence to protocol procedures specific to each study, screening for possible trial patients, eligibility criteria, and patient follow up. This position is responsible for coordination of trial activities mentioned above as well as others.</p> <p>Required Qualifications</p> <ul> <li>Require research certification within one (1) year of eligibility. </li><li>Require a minimum of five (5) years of healthcare experience with two (2) of the years being within a research role. </li><li>Require completion of Good Clinical Practice & Human Subject Protection and Safety Handling/Hazardous training within two (2) weeks of hire/transfer date.. </li></ul> <p>Preferred Qualifications</p> <ul> <li>Prefer in-depth knowledge of good clinical practices as set forth by Federal regulations. </li><li>Prefer an organized individual with strong critical thinking skills who has the ability to work efficiently under pressure. </li><li>Prefer someone who is highly motivated, shows initiative, is proactive, and able to work independently as well as in a team. </li></ul> <p>Mandatory Education</p> <p>A D: Associate's Degree</p> <p>Preferred Education</p> <p>BD: Bachelor Degree</p> <p>Required License and Certs</p> <p>Preferred License and Certs</p>