Eye Care Clinical Research Coordinator – Entry Level

American Vision Partners; Mesa (AZ); Presencial; USD 42 000 - 62 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical insurance

Dental insurance

Eye care discounts

Child care assistance

Pet insurance

Continuing education funds

401(k)

Paid holidays

PTO

Resumo da oferta

American Vision Partners seeks a Junior Clinical Research Coordinator to assist in managing all aspects of clinical trials across AVP locations. You will coordinate between investigators, study staff and sponsors, screen and enroll subjects, and ensure protocol compliance and data integrity.

You will support regulatory submissions, data entry, and adverse event reporting while traveling between RCA research offices as needed.

Qualificações

• Associate or Bachelor’s Degree expected or in progress.
• Clinical experience in Retina or optical care.
• Prior research experience.
• IATA or Human Subjects protection training or GCP training desirable.
• CRC certification or related specialty certification preferred.

Responsabilidades

• Acts as a liaison between investigators, staff, IRB and sponsor.
• Screens, consents, enrolls and follows study subjects with protocol compliance.
• Maintains data, source docs and adverse event reporting.
• Ensures regulatory documents are completed and submitted to IRB.
• Ensures proper billing communication and processing for subjects.
• Maintains trial files and timely CRF data entry.

Conhecimentos

Clinical experience Retina/optical

Prior research experience

IATA training or GCP training

CRC certification preferred

Formação académica

Associate or Bachelor’s Degree or in progress

Descrição da oferta de emprego

American Vision Partners seeks a Junior Clinical Research Coordinator to assist in managing all aspects of clinical trials across AVP locations. You will coordinate between investigators, study staff and sponsors, screen and enroll subjects, and ensure protocol compliance and data integrity.

You will support regulatory submissions, data entry, and adverse event reporting while traveling between RCA research offices as needed.