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Job description
Parexel, a global clinical development partner, is seeking a scientifically driven professional to support biospecimen and data use in clinical trials. You will review informed consent language and ensure compliance across multiple jurisdictions while partnering with leading pharma and biotech teams.
The role is full-time and fully remote, with EST hours. You will work across therapy areas on genetic and biomarker consent, biospecimen management, and precision medicine initiatives.
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Worksite address
boise, ID, 83708, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.