- Home
- Jobs
- Clinical Operations
- Associate, Clinical Operations

Associate, Clinical Operations at Priovant Therapeutics
United StatesFull-timeClinical OperationsPosted about 1 month ago
Apply with PipelineAbout the Role
<p><span class="NormalTextRun SCXW27708325 BCX0" data-ccp-parastyle="Default" data-ccp-parastyle-defn="{"ObjectId":"272499da-5523-5969-b17c-4f82c0ce3910|1","ClassId":1073872969,"Properties":[469775450,"Default",201340122,"2",134233614,"true",469778129,"Default",335572020,"1",469777841,"Times New Roman",469777842,"Times New Roman",469777844,"Times New Roman",469769226,"Times New Roman",335551500,"0",268442635,"24",335559740,"240",201341983,"0",335559739,"0",201342446,"1",201342447,"5",201342448,"1",201342449,"1",469777843,"Calibri",201341986,"1"]}">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="{}"> </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="{}"> </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="{}"> </span></li>
<li><span data-contrast="auto">Help manage site-level interfacing with external vendors, such as troubleshooting site issues </span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="auto">Support the clinical monitoring team by co-monitoring on key programs </span><span data-ccp-props="{}"> </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="{}"> </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="{"ObjectId":"272499da-5523-5969-b17c-4f82c0ce3910|1","ClassId":1073872969,"Properties":[469775450,"Default",201340122,"2",134233614,"true",469778129,"Default",335572020,"1",469777841,"Times New Roman",469777842,"Times New Roman",469777844,"Times New Roman",469769226,"Times New Roman",335551500,"0",268442635,"24",335559740,"240",201341983,"0",335559739,"0",201342446,"1",201342447,"5",201342448,"1",201342449,"1",469777843,"Calibri",201341986,"1"]}">Bachelor’s degree (preferably in a scientific or technical discipline)</span></span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li>
<li><span data-contrast="auto">Minimum of 2 years of clinical research experience – ideally 3-4 years</span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="auto">Strong organizational skill set. Ability to manage multiple tasks and competing priorities. </span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="auto">Collaborative, with the ability to work well in small teams. </span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="auto">Extremely detail-oriented</span><span data-ccp-props="{}"> </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="{}"> </span></li>
<li><span data-contrast="auto">Ability to learn quickly and respond well to feedback. </span><span data-ccp-props="{}"> </span></li>
<li><span data-contrast="auto">Proficiency with Excel, PowerPoint and project management software such as Monday.com</span><span data-ccp-props="{}"> </span></li>
</ul>
Related Roles
Contract Clinical Research Associate
Priovant Therapeutics
United StatesManager/Senior Manager, Clinical Development (in-person)
Priovant Therapeutics
North CarolinaArizona Patient Access Liaison (PAL)
Priovant Therapeutics
ArizonaAssociate, Clinical Trial Management
Lyell Immunopharma
Seattle, Washington, United StatesMedical Assistant
Spring Fertility
New York, New YorkClinical Engagement Regional Associate Director (Europe & Asia)
Beeline Medicines
United Kingdom