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Associate Specialist, Clinical Trials Operations

LifelancerUnited States🌍 Remote
Full-timeMid Level
$0k - $0k
per year
👁️ 0 views📝 0 applicationsPosted 8/9/2026Expires 10/8/2026
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Job Description

Job Title: Associate Specialist, Clinical Trials Operations Job Location: US CA San Diego, United States of America Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Who We Are: Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs.

We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders.

The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas.

For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science.

For more information, visit neurocrine. com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)

About the Role

Supports and assists the centralized operational activities for assigned Clinical Studies.

Centralized activities can include but are not limited to set up of studies, development of Informed Consent documents and study plans, handling IRB submissions of protocol/ICF/sites, management of the Trial Master File (TMF) and Financial Disclosure Forms, feasibility and selection of sites, coordination of committees (i.

e. adjudication committees), support of site enrollment, and oversight of monitoring for studies outsourced to Contract Research Organizations (CROs). _ Your Contributions (include, but are not limited to): Assists to ensure

Required Skills

Clinical Trials OperationsInformed ConsentIRB submissionsTrial Master FileFinancial Disclosure Formssite feasibilitysite selectionsite enrollmentmonitoringContract Research Organizations

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