Ophthalmology Clinical Research Coordinator - Onsite Mon-Fri

Medix; Edison (NJ); On-site; USD 44,000 - 52,000; Full time

Job summary

Medix is seeking a Clinical Research Professional for an ophthalmology study, on-site, full-time, with responsibilities including patient visits, phlebotomy, and data entry across EDC systems. You will collaborate with clinic staff and monitors to ensure study progress and regulatory compliance.

The role requires independent work capability, strong communication, and retinal/anterior segment knowledge. Competitive salary and benefits follow 30 days after hire, with a focus on accurate data

Qualifications

• Certified for phlebotomy / blood draws.
• Hands-on experience operating a centrifuge for specimen processing.
• Background in Ophthalmology, specifically Retina, Anterior Segment, or general eye care.
• Proficiency in data entry across various Electronic Data Capture (EDC) platforms.
• Standard clinical research regulatory maintenance and audit readiness.
• Understanding of IP accountability and monitoring processes.
• Proven ability to work independently ("plug-and-play") without direct daily onsite supervision.
• Strong interpersonal skills to interface with clinic staff and investigators.

Responsibilities

• Manage 1-3 patient visits per day with admin days during new study launches.
• Perform certified phlebotomy and operate centrifuges for specimen processing.
• Coordinate with onsite clinic staff and monitors to ensure smooth study flow.
• Input clinical trial data across EDC platforms in a timely manner.
• Maintain regulatory binders and study documentation to audit standards.
• Oversee IP processes and host external study monitors.

Skills

Phlebotomy

Centrifuge operation

Ophthalmology knowledge

EDC data entry

Regulatory compliance

IP accountability

Independent work

Interpersonal communication

Tools

EDC platforms

Job description

Medix is seeking a Clinical Research Professional for an ophthalmology study, on-site, full-time, with responsibilities including patient visits, phlebotomy, and data entry across EDC systems. You will collaborate with clinic staff and monitors to ensure study progress and regulatory compliance.

The role requires independent work capability, strong communication, and retinal/anterior segment knowledge. Competitive salary and benefits follow 30 days after hire, with a focus on accurate data