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Job description
Ora Inc. is seeking a Clinical Trial Associate I to support project managers and study teams in ophthalmic clinical research.
The role covers study start-up, maintenance, and close-out activities, ensuring GCP compliance and proper regulatory documentation across sites. The candidate will handle site coordination, regulatory packages, CTMS/eTMF duties, and data collection while working in a semi-virtual, cross-functional environment.
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Worksite address
union, NJ, 07083, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.