Ophthalmic Clinical Research Coordinator

Paycom - ATS; Pasadena (CA); On-site; USD 70,000 - 95,000; Full time

Job summary

Azul Vision is seeking a Clinical Research Coordinator to support principal investigators in ophthalmic clinical trials in Southern California. You will oversee patient care, ensure protocol adherence, and manage regulatory documentation in a fast-paced clinic.

Responsibilities include coordinating with sponsors, obtaining informed consent, maintaining accurate data, and training staff to comply with GCP guidelines. Strong MS Office skills and organizational abilities are essential.

Qualifications

• High School Diploma or GED required.
• Bachelor's degree preferred.
• Experience in clinical research or ophthalmic setting is advantageous.

Responsibilities

• Interpret, comprehend, and conduct clinical research procedures per protocol.
• Oversee all aspects of patients involved in clinical trials.
• Coordinate informed consent discussions with patients and families.
• Prepare IRB submissions and ensure regulatory compliance.
• Coordinate site visits with sponsors and maintain delegation logs.
• Collect, record, and report study data accurately.
• Perform ophthalmic assessments and related procedures as required.
• Train staff to ensure protocol compliance.

Skills

Organizational skills

Communication skills

Written communication

Microsoft Office

Analytical skills

Time management

Education

High School Diploma or GED

Bachelor's degree preferred

Tools

Microsoft Office

Job description

Azul Vision is seeking a Clinical Research Coordinator to support principal investigators in ophthalmic clinical trials in Southern California. You will oversee patient care, ensure protocol adherence, and manage regulatory documentation in a fast-paced clinic.

Responsibilities include coordinating with sponsors, obtaining informed consent, maintaining accurate data, and training staff to comply with GCP guidelines. Strong MS Office skills and organizational abilities are essential.