Associate Clinical Research Coordinator, Ophthalmology
2 weeks ago
Associate Clinical Research Coordinator, Ophthalmology
The Clinical Research Coordinator (CRC) will work closely with the Principal Investigator (PI), study team members, Research Director, Research Manager and supporting teams to ensure the successful planning, execution, and completion of clinical trials and research projects. The CRC will play a key role in participant recruitment, data management, and regulatory compliance, contributing to impactful clinical research.
Job Responsibilities
Plan, coordinate, and execute clinical research studies from initiation to close-out, ensuring adherence to study protocols and timelines.
Screen, recruit, and enrol eligible study participants, obtaining informed consent in accordance with ethical and regulatory requirements.
Collect, manage, and analyze study data in line with protocol requirements and regulatory standards, ensuring data integrity and accuracy.
Maintain comprehensive and organized study documentation, including regulatory binders, case report forms, and participant records.
Collaborate with study sponsors, regulatory authorities, and study sites to ensure ongoing compliance and efficient study progress.
Manage study drug and device inventory, ensuring proper storage, handling, and accountability.
Monitor and report adverse events, protocol deviations, and other critical issues to study sponsors and regulatory authorities as required.
Assist in the preparation and submission of study progress reports, regulatory submissions, and ethics applications.
Ensure full compliance with Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
Support the Research Manager in grant planning, budget verification, cost assessments, monthly invoicing, and
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