Travel-Ready Eye Care Clinical Research Coordinator

Azul Vision, Inc.

Pasadena (CA)

On-site

USD 60,000 - 80,000

Full time

12 days ago

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Job summary

Azul Vision, Inc. in Pasadena, CA is seeking a Clinical Research Coordinator to support ophthalmic trials within a busy clinic environment.

You will work with principal investigators to recruit, screen, consent, and monitor patients, while ensuring strict adherence to trial protocols and regulatory requirements. The role involves coordinating site visits, maintaining study files, performing imaging, and training staff to ensure compliance with GCP and sponsor expectations.

Qualifications

  • High School Diploma or GED required.
  • Bachelor's degree preferred.
  • Minimum of 2 years of experience in the clinical research industry.
  • Prior ophthalmic technician experience is highly desired.
  • Through knowledge of eye anatomy, disease, symptoms, and ocular medications.

Responsibilities

  • Interpret, comprehend, and conduct clinical research procedures while following all protocols.
  • Oversee all aspects of patients involved in clinical trials.
  • Pre-screen detailed chart review of potential patient records.
  • Coordinate site visits with Sponsors to ensure professional representation.
  • Prepare and ensure accurate IRB submissions, including safety reports.
  • Perform ophthalmic examinations and imaging (OCT, Fundus, FA) as part of data collection.
  • Data collection, documentation, entry, and sponsor query responses.

Skills

Organizational skills
Communication skills
Microsoft Office
Analytical skills
Judgment

Education

High School Diploma or GED
Bachelor’s degree preferred

Job description

Azul Vision, Inc. in Pasadena, CA is seeking a Clinical Research Coordinator to support ophthalmic trials within a busy clinic environment.

You will work with principal investigators to recruit, screen, consent, and monitor patients, while ensuring strict adherence to trial protocols and regulatory requirements. The role involves coordinating site visits, maintaining study files, performing imaging, and training staff to ensure compliance with GCP and sponsor expectations.

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