# Clinical Trial Associate I at Ora

- Company: Ora
- What the company does: At ORA, we believe that health & wellbeing should be more accessible, convenient & personal. Backed by Antler.
- Company website: https://www.ora.group/
- Type: Startups
- Level: Associate
- Location: Remote - EU
- Work setup: Remote
- Posted: 2026-09-24
- Apply by: 2026-11-08
- Apply: https://job-boards.greenhouse.io/ora/jobs/4716265006
- Page: https://www.1752.vc/careers/jobs/ora-clinical-trial-associate-i/

## About the role

Ora’s Clinical Trial Associate I (CTA I) assists Project Managers and study teams in clinical study conduct for clinical ophthalmic projects. They support the oversight feasibility including but not limited to, working with sites to generate contracts and budgets, collecting regulatory documents, and may be involved in scheduling follow up patient visits of all clinical sites and ensures compliance with (GCP) protocol along with overall clinical objectives.

## What they're looking for

- Ensure study documentation, communication, training and data collection is aligned with study protocol adherence, and all applicable SOPs, regulations and guidelines
- Drafts and/or reviews study-related documents and templates including study protocols, informed consents, source document templates, study plans, study related logs, etc
- Participate in study start-up (including Investigator Meeting), study maintenance and study closeout activities
- Collect and review site regulatory documents for accuracy and completion (e.g., 1572, Financial Disclosure documents, CLIA waivers, etc.)
- Prepare, with oversight, essential documents package to support investigational product release for study and site approval
- Create regulatory packages for IRB/IEC submission for study and site initial submission as well as applicable study and site continuity report submissions and close-out submissions

Tags: Ora Europe