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Job description
ProPharma is seeking a Central Monitoring Associate to support clinical monitoring teams using centralized data tools in accordance with SOPs and regulatory guidelines. The role emphasizes remote site management, data reporting, and adherence to quality standards.
Candidates should have a bachelor’s degree (preferred) and at least 3 years in study coordination or in-house monitoring within biotech or pharma. Hybrid work arrangement available, with opportunities for collaboration across offices.
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Worksite address
raleigh, NC, 27601, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.