Intern, Clinical Regulatory Writing
UltraGenix PharmaceuticalUnited States - RemotePosted 5 March 2026
Job Description
<div class="content-intro"><div><strong>Why Join Us?</strong></div>
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<div><em>Be a hero for our rare disease patients</em></div>
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<div>At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won’t go – challenging the status quo and creating a new model that advances our field so more patients and caregivers can benefit from life-changing treatments. We do this by following the science, applying a novel rapid development approach, making innovative medicines at fair and reasonable prices, and creating a collaborative ecosystem to reach patients in ways that are most meaningful for them. </div>
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<div>Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth – so employees can thrive in all areas of their lives, in and outside of work. Ultimately, we want to be an organization where we would be proud for our family, friends and children to work.</div>
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<div>If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team<em>. </em></div></div><h3 style="text-align: left;"><strong>Position Summary:</strong></h3>
<p style="text-align: left;"><em><strong>ultra</strong>dedicated – Your biggest challenges yield rare possibilities</em></p>
<p style="text-align: left;"><span class="TextRun SCXW142468857 BCX8" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW142468857 BCX8">This is a unique opportunity for</span><span class="NormalTextRun SCXW142468857 BCX8"> either</span><span class="NormalTextRun SCXW142468857 BCX8"> </span><span class="NormalTextRun ContextualSpellingAndGrammarErrorV2Themed SCXW142468857 BCX8">master's</span><span class="NormalTextRun SCXW142468857 BCX8"> </span><span class="NormalTextRun SCXW142468857 BCX8">or</span><span class="NormalTextRun SCXW142468857 BCX8"> PhD </span><span class="NormalTextRun SCXW142468857 BCX8">students to support the clinical regulatory writing team in the </span><span class="NormalTextRun SCXW142468857 BCX8">clinical</span><span class="NormalTextRun SCXW142468857 BCX8"> development of treatments for rare and ultra-rare diseases. The clinical regulatory writing intern will work closely with the medical writing and cross-functional teams to develop high quality clinical and regulatory documents for global marketing applications. </span></span><span class="EOP SCXW142468857 BCX8" data-ccp-props="{"201341983":0,"335559740":256}"> </span></p>
<h3 style="text-align: left;"><strong>Work Model: </strong></h3>
<p style="text-align: left;">Remote: Officially documented as working full-time from home, with travel to Ultragenyx's offices or other locations on occasion as needed.</p>
<h3 style="text-align: left;"><strong>Responsibilities:</strong></h3>
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<li style="line-height: 2;"><span data-contrast="auto">Participate in the authoring and review of clinical and regulatory documents relating to global marketing applications and clinical trials (eg, clinical study reports, protocols, safety narratives)</span><span data-ccp-props="{"201341983":0,"335559685":900,"335559739":200,"335559740":276,"335559991":558}"> </span></li>
<li style="line-height: 2;"><span data-contrast="auto">Learn and apply medical writing standards</span><span data-ccp-props="{"201341983":0,"335559685":900,"335559739":200,"335559740":276,"335559991":558}"> </span></li>
<li style="line-height: 2;"><span data-contrast="auto">Understand the process of distilling large amounts of clinical and scientific data into essential elements for tabular and graphical display</span><span data ... (truncated, view full listing at source)
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