Ophthalmology CRC – Growth & CE Funds

jobs-americanvisionpartners; Phoenix (AZ); On-site; USD 52,000 - 72,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Eye care discounts

Child care assistance

Pet insurance

Continuing education funds

401(k)

Paid holidays

PTO

Sick Time

Growth opportunities

Job summary

American Vision Partners in Phoenix seeks a Junior Clinical Research Coordinator to assist in managing clinical trials across ophthalmology practices. You will coordinate consent, enrollment, and follow-up while ensuring protocol compliance and data integrity in a dynamic clinical setting.

The role involves regulatory documentation, IRB submissions, and collaboration with investigators and study staff to deliver high-quality patient care and research outcomes.

Qualifications

• Clinical research experience in Retina or related optical care is preferred.
• Experience with regulatory documents and IRB submissions is desirable.
• GCP/IATA training or Human Subjects protection training is advantageous.

Responsibilities

• Act as liaison between investigators, study staff, providers, IRB and sponsor.
• Screen, enroll, consent and monitor subjects per protocol with data accuracy and safety.
• Manage source documents, adverse event reporting, and regulatory filings.
• Coordinate billing for research subjects and communicate procedure costs.
• Prepare study materials for IRB submissions and audits.
• Maintain regulatory documents and attend study visits and meetings.
• Ensure adherence to protocol and accurate data entry in sponsor databases.
• Oversee drug administration, storage, and accountability; ensure patient safety.

Skills

Clinical research

Retina experience

Regulatory training

GCP/IATA training

CCRC certification

Education

Associate or Bachelor’s Degree

Job description

American Vision Partners in Phoenix seeks a Junior Clinical Research Coordinator to assist in managing clinical trials across ophthalmology practices. You will coordinate consent, enrollment, and follow-up while ensuring protocol compliance and data integrity in a dynamic clinical setting.

The role involves regulatory documentation, IRB submissions, and collaboration with investigators and study staff to deliver high-quality patient care and research outcomes.