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Priovant Therapeutics

Associate, Clinical Operations at Priovant Therapeutics

United StatesFull-timeClinical OperationsPosted about 1 month ago
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About the Role

<p><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default" data-ccp-parastyle-defn="{&quot;ObjectId&quot;:&quot;272499da-5523-5969-b17c-4f82c0ce3910|1&quot;,&quot;ClassId&quot;:1073872969,&quot;Properties&quot;:[469775450,&quot;Default&quot;,201340122,&quot;2&quot;,134233614,&quot;true&quot;,469778129,&quot;Default&quot;,335572020,&quot;1&quot;,469777841,&quot;Times New Roman&quot;,469777842,&quot;Times New Roman&quot;,469777844,&quot;Times New Roman&quot;,469769226,&quot;Times New Roman&quot;,335551500,&quot;0&quot;,268442635,&quot;24&quot;,335559740,&quot;240&quot;,201341983,&quot;0&quot;,335559739,&quot;0&quot;,201342446,&quot;1&quot;,201342447,&quot;5&quot;,201342448,&quot;1&quot;,201342449,&quot;1&quot;,469777843,&quot;Calibri&quot;,201341986,&quot;1&quot;]}">Priovant is committed to developing therapies that address high unmet need in autoimmune disease. </span><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default">The Associate, Clinical Operations will help advance this mission by driving operational</span><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default"> and monitoring</span><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default"> execution on </span><span class="NormalTextRun SpellingErrorV2Themed SCXW27708325 BCX0" data-ccp-parastyle="Default">Priovant’s</span><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default"> late-stage clinical trials, ensuring that the most important projects at the company are </span><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default">accomplished</span><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default"> successfully</span><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default">.</span></p> <p><strong><span class="TextRun SCXW98714338 BCX0" lang="EN-US" data-contrast="none"><span class="NormalTextRun SCXW98714338 BCX0" data-ccp-parastyle="Default">Responsibilities</span></span></strong></p> <ul> <li><span data-contrast="auto">Develop and maintain a system for organizing and tracking essential documents related to study start-up and execution</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Function as the first-round reviewer of IP release checklists, ensuring that all essential study documents meet compliance standards prior to site activation</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Support the timely execution of Priovant’s clinical development goals by managing and maintaining key study metrics around monitoring and data quality</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Help manage site-level interfacing with external vendors, such as troubleshooting site issues&nbsp;</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Support the clinical monitoring team by co-monitoring on key programs&nbsp;</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Facilitate tracking of operational on-study workflows, such as protocol amendment implementation and patient re-consenting</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Ad hoc support for clinical operations workstreams across programs</span></li> </ul> <p><strong><span data-ccp-props="{}">Qualifications</span></strong></p> <ul> <li><span data-contrast="none"><span data-ccp-parastyle="Default" data-ccp-parastyle-defn="{&quot;ObjectId&quot;:&quot;272499da-5523-5969-b17c-4f82c0ce3910|1&quot;,&quot;ClassId&quot;:1073872969,&quot;Properties&quot;:[469775450,&quot;Default&quot;,201340122,&quot;2&quot;,134233614,&quot;true&quot;,469778129,&quot;Default&quot;,335572020,&quot;1&quot;,469777841,&quot;Times New Roman&quot;,469777842,&quot;Times New Roman&quot;,469777844,&quot;Times New Roman&quot;,469769226,&quot;Times New Roman&quot;,335551500,&quot;0&quot;,268442635,&quot;24&quot;,335559740,&quot;240&quot;,201341983,&quot;0&quot;,335559739,&quot;0&quot;,201342446,&quot;1&quot;,201342447,&quot;5&quot;,201342448,&quot;1&quot;,201342449,&quot;1&quot;,469777843,&quot;Calibri&quot;,201341986,&quot;1&quot;]}">Bachelor’s degree (preferably in a scientific or technical discipline)</span></span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:0,&quot;335559740&quot;:240}">&nbsp;</span></li> <li><span data-contrast="auto">Minimum of 2 years of clinical research experience – ideally 3-4 years</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Strong organizational skill set. Ability to manage multiple tasks and competing priorities.&nbsp;</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Collaborative, with the ability to work well in small teams.&nbsp;</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Extremely detail-oriented</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Flexibility to travel when needed (may support up to 2 on-site visits each month)</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Ability to learn quickly and respond well to feedback.&nbsp;</span><span data-ccp-props="{}">&nbsp;</span></li> <li><span data-contrast="auto">Proficiency with Excel, PowerPoint and project management software such as Monday.com</span><span data-ccp-props="{}">&nbsp;</span></li> </ul>