Ophthalmic Clinical Trials Associate I

Ora Inc.; Union, Northern (NJ, KY); Hybrid; USD 55,000 - 75,000; Full time

Job summary

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.

Qualifications

• Bachelor’s Degree with at least 1 year of research experience.
• Clinical trial experience strongly preferred; ophthalmic experience is a plus.

Responsibilities

• Assist Project Managers and study teams in clinical study conduct for ophthalmic projects.
• Support feasibility activities including working with sites to generate contracts and budgets; collect regulatory documents; assist in scheduling follow-up visits.

Skills

Clinical trial experience

Ophthalmic experience

GCP/ICH regulations

CTMS/eTMF familiarity

Documentation & communication

Analytical skills

Semi-virtual teamwork

Multilingual (plus)

Education

Bachelor’s Degree in Life Sciences

Tools

CTMS

eTMF

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.