Ophthalmic Clinical Trial Associate
Listed on 2026-10-02
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Healthcare
Clinical Research
Ora Europe is seeking a Clinical Trial Associate I to support project managers and study teams across ophthalmic clinical trials. The role involves regulatory document collection, site budgeting, and document preparation to ensure study startup, maintenance, and closeout activities are compliant with GCP.
The CTA I will help maintain the Trial Master File, assist with CTMS, and support audits and regulatory submissions while traveling up to 10% as needed.
Consider building your career as a Ophthalmic Clinical Trial Associate I at Ora.
Step into the Ophthalmic Clinical Trial Associate I role at Ora in United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
This is a Full Time role.
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