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Senior Clinical Trial Specialist (Contract)

Centessapharmaceuticalsinc • Boston, MA

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> </p> <p><strong>Description of Role</strong></p> <p><span class="TextRun SCXW192947886 BCX0" lang="EN-US" data-contrast="none"><span class="NormalTextRun SCXW192947886 BCX0">The</span><span class="NormalTextRun SCXW192947886 BCX0"> (contract-to-hire)</span><span class="NormalTextRun SCXW192947886 BCX0"> Sr. Clinical Trial </span><span class="NormalTextRun SCXW192947886 BCX0">Specialist</span> <span class="NormalTextRun ContextualSpellingAndGrammarErrorV2Themed SCXW192947886 BCX0">perform</span><span class="NormalTextRun SCXW192947886 BCX0"> tasks to support the planning and execution of clinical studies across one or more clinical trials. </span><span class="NormalTextRun SCXW192947886 BCX0">This role is a temporary position with the potential to convert to a permanent rol</span><span class="NormalTextRun SCXW192947886 BCX0">e, </span><span class="NormalTextRun SCXW192947886 BCX0">work</span><span class="NormalTextRun SCXW192947886 BCX0">ing</span><span class="NormalTextRun SCXW192947886 BCX0"> closely</span><span class="NormalTextRun SCXW192947886 BCX0"> with the Clinical Trial Manager (CTM) to ensure site start-up through close-out activities are conducted </span><span class="NormalTextRun SCXW192947886 BCX0">in accordance with</span><span class="NormalTextRun SCXW192947886 BCX0"> Standard Operating Procedures (SOPs), GCP and regulatory guidelines. </span></span><span class="EOP Selected SCXW192947886 BCX0" data-ccp-props="{"134233117":true,"134233118":true,"201341983":0,"335559740":240}"> </span></p> <p><strong>Key Responsibilities</strong></p> <ul> <li data-leveltext="" data-font="Symbol" data-listid="2" data-list-defn-props="{"335552541":1,"335559685":360,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":"","469777815":"multilevel"}" data-aria-posinset="1" data-aria-level="1"><span data-contrast="none">Assists and provides support to the CTM and study team in the day-to-day operational management of assigned clinical trials.</span></li> <li data-leveltext="" data-font="Symbol" data-listid="2" data-list-defn-props="{"335552541":1,"335559685":360,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":"","469777815":"multilevel"}" data-aria-posinset="1" data-aria-level="1">Supports the CTM in coordination, preparation, and documentation of internal and external meetings such as Kick-Off Meetings, Investigator Meetings, and vendor management meetings by preparing agendas, minutes, and presentation materials, organizing meeting logistics and travel arrangements if necessary.</li> <li data-leveltext="" data-font="Symbol" data-listid="2" data-list-defn-props="{"335552541":1,"335559685":360,"335559991":360,"469769226":"Symbol","4

Job Reference ID: CF-172724 • Posted on CloudFrame Job Scanner