Clinical Research Coordinator, Ophthalmology - 238828

Medix™; Seattle (WA); On-site; Full time

Job summary

An established industry player is seeking a dedicated Clinical Research Coordinator to join their Ophthalmology Research Department. This full-time, on-site role offers a unique opportunity to contribute to groundbreaking research that enhances vision science and patient care. As a key player in coordinating clinical studies, you will ensure compliance with regulatory standards while managing participant enrollment and study documentation. If you are detail-oriented and passionate about making a difference in the field of ophthalmology, this position is perfect for you. Join a team of leading researchers and clinicians and help advance the future of eye care.

Qualifications

• 3+ years of experience as a Clinical Research Coordinator required.
• Strong knowledge of regulatory compliance and GCP essential.

Responsibilities

• Manage multiple ophthalmology clinical research studies from start to finish.
• Screen, recruit, and enroll participants while ensuring compliance.

Skills

Clinical Research Coordination

Regulatory Compliance

Good Clinical Practice (GCP)

Communication Skills

Organizational Skills

Problem-Solving Skills

Education

Bachelor's Degree

Associate's Degree

Tools

Microsoft Office

Electronic Data Capture Systems

Job description

Clinical Research Coordinator, Ophthalmology - 238828

Clinical Research Coordinator – Ophthalmology Research

Location: Seattle, WA (On-site)

Schedule: Monday – Friday

Compensation: $35 - $40 per hour

Position Overview

We are seeking a dedicated and experienced Clinical Research Coordinator (CRC) to join our Ophthalmology Research Department at a leading academic institution in Seattle, WA. The CRC will play a crucial role in supporting clinical research studies by coordinating study activities, ensuring compliance with regulatory requirements, and facilitating participant enrollment. This is a full-time, on-site position.

Key Responsibilities

• Coordinate and manage multiple ophthalmology clinical research studies from initiation to closeout.
• Screen, recruit, and enroll study participants, ensuring informed consent is obtained.
• Schedule and conduct study visits, collect data, and maintain accurate research records.
• Adhere to study protocols and ensure compliance with IRB, FDA, and institutional guidelines.
• Monitor study progress, address deviations, and report adverse events as required.
• Serve as the primary liaison between investigators, sponsors, study participants, and regulatory agencies.
• Maintain and update study documentation, including case report forms (CRFs) and electronic databases.
• Assist with grant applications, budgets, and financial tracking for research projects.

Qualifications

• Minimum of 3 years of experience as a Clinical Research Coordinator.
• Bachelor's or Associate's degree preferred (equivalent experience will be considered).
• Strong understanding of Good Clinical Practice (GCP), regulatory compliance, and IRB processes.
• Experience with ophthalmology research or medical research preferred but not required.
• Excellent communication, organizational, and problem-solving skills.
• Proficiency in Microsoft Office and electronic data capture systems.
• Ability to work independently and collaboratively in a fast-paced academic research setting.

Why Join Us?

This role offers the opportunity to contribute to cutting-edge ophthalmology research at a prestigious academic institution. You will work alongside leading researchers and clinicians, supporting studies that advance vision science and improve patient care.

If you are a detail-oriented and motivated Clinical Research Coordinator looking to make an impact, we encourage you to apply!

Seniority level

Associate

Employment type

Contract

Job function

Research and Health Care Provider

Industries

Research Services and Hospitals and Health Care