Retina Clinical Research Coordinator — Drive Eye Care Trials

Medix™; Modesto (CA); Presencial; USD 65.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

PTO 13 days/year

7 paid holidays

401(k) plan

Descripción de la vacante

Medix is seeking a full-time Clinical Research Coordinator in Modesto, CA to join our retina-focused clinical research team. The coordinator will manage day-to-day trial visits, ensure adherence to ICH-GCP and IRB requirements, and collaborate with physicians, staff, and pharmaceutical sponsors.

The ideal candidate has 2+ years of clinical research experience or CRCC/CCRP certification, with strong communication and meticulous documentation skills.

Formación

• 2+ years of clinical research experience or CRCC/CCRP certification.
• Strong written and verbal communication skills.
• Ability to work independently while collaborating with a multidisciplinary team.

Responsabilidades

• Coordinate day-to-day clinical trial activities and patient visits.
• Review study protocols, timelines and eligibility criteria.
• Screen and recruit participants and support enrollment goals.
• Conduct informed consent and ensure documentation.
• Maintain source documentation and study files.
• Enter data in EDC systems and resolve data queries.

Conocimientos

Clinical research

IRB process

ICH-GCP

Patient interaction

Documentation

Educación

High school diploma or equivalent

CRCC/CCRP certification

Herramientas

Ophthalmic equipment

EDC systems

Descripción del empleo

Medix is seeking a full-time Clinical Research Coordinator in Modesto, CA to join our retina-focused clinical research team. The coordinator will manage day-to-day trial visits, ensure adherence to ICH-GCP and IRB requirements, and collaborate with physicians, staff, and pharmaceutical sponsors.

The ideal candidate has 2+ years of clinical research experience or CRCC/CCRP certification, with strong communication and meticulous documentation skills.