Clinical Trial Manager (Contract)
Job Description
<div class="content-intro"><p><em>Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, </em><em>is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa’s lead investigational candidate – cleminorexton (formerly ORX750) – is being developed for narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions.</em></p> <p><em> </em><em>Headquartered in Boston, Massachusetts, Centessa was recognized as a <strong>Great Place to Work</strong>® in 2026.</em></p></div><p><strong>Description of Role</strong></p> <p><span class="TextRun SCXW116178689 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW116178689 BCX0">Centessa is seeking </span><span class="NormalTextRun SCXW116178689 BCX0">a </span><span class="NormalTextRun SCXW116178689 BCX0">(contract to hire) </span><span class="NormalTextRun SCXW116178689 BCX0">Clinical Trial Manager to</span><span class="NormalTextRun SCXW116178689 BCX0"> lead the execution of mid</span></span><span class="NoBreakHyphenBlob BlobObject DragDrop SCXW116178689 BCX0">‑</span><span class="TextRun SCXW116178689 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW116178689 BCX0"> to late</span></span><span class="NoBreakHyphenBlob BlobObject DragDrop SCXW116178689 BCX0">‑</span><span class="TextRun SCXW116178689 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW116178689 BCX0">stage global clinical studies from study start</span></span><span class="NoBreakHyphenBlob BlobObject DragDrop SCXW116178689 BCX0">‑</span><span class="TextRun SCXW116178689 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW116178689 BCX0">up through close</span></span><span class="NoBreakHyphenBlob BlobObject DragDrop SCXW116178689 BCX0">‑</span><span class="TextRun SCXW116178689 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW116178689 BCX0">out and clinical study report.</span> <span class="NormalTextRun SCXW116178689 BCX0">This role is a temporary position with the potential to convert to a permanent role,</span> <span class="NormalTextRun SCXW116178689 BCX0">responsible</span><span class="NormalTextRun SCXW116178689 BCX0"> for day</span></span><span class="NoBreakHyphenBlob BlobObject DragDrop SCXW116178689 BCX0">‑</span><span class="TextRun SCXW116178689 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW116178689 BCX0">to</span></span><span class="NoBreakHyphenBlob BlobObject DragDrop SCXW116178689 BCX0">‑</span><span class="TextRun SCXW116178689 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW116178689 BCX0">day trial management, coordinating internal cross</span></span><span class="NoBreakHyphenBlob BlobObject DragDrop SCXW116178689 BCX0">‑</span><span class="TextRun SCXW116178689 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW116178689 BCX0">functional teams and overseeing CROs and external vendors to ensure studies are delivered on time, within budget, and in compliance with quality and regulatory standards. This role requires hands</span></span><span class="NoBreakHyphenBlob BlobObject DragDrop SCXW116178689 BCX0