Clinical Research Coordinator, Ophthalmology

2 weeks ago


Singapur, Singapore National University Hospital Full time

Overview

The Department of Ophthalmology is seeking a Clinical Research Coordinator to support retina-focused clinical research studies. This role coordinates and manages retina-related clinical studies from initiation to close-out, ensuring adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements.

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 line with ethical and regulatory requirements.
  • Collect, manage, and analyze study data in accordance 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 GCP guidelines and all applicable regulatory requirements.
  • Support the Research Manager in grant planning, budget verification, cost assessments, monthly invoicing, and account management.
  • Contribute to department events, ad-hoc projects, and other administrative duties as needed.
  • Ensure timely follow-up and completion of all assigned tasks within stipulated deadlines.
Qualifications
  • Registered Optometrist with the Singapore Optometrists & Opticians Board (OOB).
  • First degree with good results; experience in research preferred.
  • Basic understanding of statistical analysis is preferred.
  • Ability to work independently and in a team, with an investigative nature and attention to detail.
  • Knowledge of computer applications, e.g., SPSS, MS Office, PowerPoint.
  • Prior experience in clinical research or healthcare is advantageous.
  • Strong organizational skills and attention to detail.
  • Effective communication and interpersonal skills for engaging with participants, team members, and external collaborators.
  • Familiarity with GCP, clinical trial processes, and relevant regulatory standards.
Senioriy
  • Entry level
Employment type
  • Contract
Job function
  • Research
Industries
  • Hospitals and Health Care
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