Clinical Research Coordinator - 244705

We are a leading clinical research organization dedicated to advancing ophthalmic science and patient care. Our team is committed to conducting ethical, high-quality studies in strict adherence to ICH-GCP guidelines and IRB-approved protocols.

Position Overview

As the Clinical Research Coordinator, you will be the cornerstone of our clinical trial operations—responsible for coordinating patient visits in alignment with ICH-GCP standards and protocol requirements. You’ll collaborate across teams to ensure compliance, data integrity, and participant safety.

Key Responsibilities

• Coordinate and facilitate daily clinical trial activities according to ICH-GCP and IRB-approved protocols.
• Administer sponsor-required questionnaires (e.g., VFQ).
• Collaborate with supply coordinators to ensure sufficient inventory of kits, shippers, and other essentials.
• Train study staff on protocol procedures, informed consent, and manuals, and ensure documentation of training.
• Create and maintain thorough source documents for each trial.
• Attend teleconferences and Investigator Meetings as directed by the Research Director.
• Review and interpret study protocols, timelines, inclusion / exclusion criteria, and confidentiality / privacy procedures.
• Partner with study and clinical teams to recruit, screen, and document eligibility of study participants.

Minimum Qualifications

Education :

• College degree preferred, but significant relevant experience will also be considered.
• Ophthalmic experience is a plus.

Experience / Skills :

• RA III level : 1–3 years of relevant clinical research coordination experience, or demonstrated excellence in prior performance evaluations.
• Strong oral and written communication.
• Ability to deliver safe, protocol-compliant care to study participants.

Certifications / Training :

• ICH-GCP Training and Certificate required.
• IATA Certification required.

Why Join Us?

• Collaborate within a driven and mission-focused clinical research team.
• Play a vital role in advancing ophthalmic clinical research in a dynamic, growing city.
• Opportunity for professional growth and impact through high-quality data, compliance, and protocol execution.