Senior Ophthalmology CRA

Responsibilities

• Build and maintain strong relationships with Principal Investigators, study coordinators, pharmacists, and site personnel to ensure efficient clinical trial execution
• Support site start-up activities, including preparation of essential documents and assistance with regulatory and ethics submissions in collaboration with IHCRA and RSU teams
• Maintain site readiness for audits and inspections while providing regular updates, reports, and issue escalation to project leadership
• Monitor clinical trial sites in accordance with ICH-GCP guidelines and Clinical Monitoring Plans, conducting visits such as initiation, routine monitoring, and close-out (onsite and remote)
• Drive patient recruitment efforts by developing and executing site-specific recruitment strategies to meet enrollment targets
• Verify accuracy and completeness of trial data, ensuring timely resolution of CRF queries and proper documentation within clinical trial systems and TMFM

Qualifications

• Bachelor’s degree in a clinical or life sciences-related field, with a preferred focus in Ophthalmology; equivalent experience in allied professions may also be considered
• Minimum of 3–5 years of Clinical Research Associate experience within the clinical research industry
• Strong time management skills with the ability to prioritize multiple studies and meet strict deadlines
• Exceptional attention to detail, ensuring accuracy and compliance with clinical protocols and regulatory requirements
• Ability to work effectively both independently and collaboratively within cross-functional, global teams
• Proficiency with clinical systems and standard software tools (e.g., CTMS, EDC, Microsoft Office)
• Prior experience in the pharmaceutical, biotechnology, or clinical research industry strongly preferred