Clinical Research Coordinator – M.Optom

We are looking for a motivated and passionate Optometrist to join our Clinical Research team as a Clinical Research Coordinator (CRC). This role offers an excellent opportunity to gain hands-on experience in clinical trial management, regulatory processes, and Good Clinical Practice (GCP) guidelines while working closely with leading ophthalmic surgeons and research professionals.
The candidate will play a key role in coordinating and monitoring clinical studies, ensuring compliance with regulatory and ethical requirements, and supporting overall clinical research activities.
Key Responsibilities
Preparation and maintenance of study protocols and Case Report Forms (CRF).
Coordinate with Ethics Committees for study submissions and approvals.
Communicate and coordinate with Principal Investigators (PI) and study coordinators across study sites.
Conduct and manage clinical trials in compliance with ICH-GCP and regulatory guidelines.
Visit study centers for monitoring and coordination activities.
Collect, review, and maintain clinical study data and documentation.
Ensure proper maintenance of study supplies and CRF documentation.
Provide regular study updates and progress reports to the reporting manager.
Support overall study monitoring and clinical trial operations.
Required Skills
Good understanding of clinical research processes and documentation.
Knowledge of ICH-GCP guidelines and regulatory requirements.
Strong communication and coordination skills.
Attention to detail and documentation accuracy.
Willingness to travel to study centers as required.
Ability to work collaboratively with cross-functional teams.
Eligibility Criteria
Education: Master of Optometry (M.Optom)
Experience: 0 to 2 years of experience in the clinical research field preferred.
Preferred Attributes
Passion for ophthalmic clinical research.
Strong organizational and interpersonal skills.
Ability to manage multiple tasks and timelines effectively.