Clinical Research Associate

IRE • Us, CA

2d

About The Position

As a Clinical Research Associate I at ICON Strategic Solutions, you will work in a sponsor-dedicated model and contribute to clinical trial operations across clinical programs. The client is seeking candidates with experience monitoring ophthalmology trials or multiple therapeutic areas. The role involves delivering clinical trial monitoring work to a high standard in collaboration with the team and stakeholders.

Requirements

• University degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines.
• Ability to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Good social skills and ability to address queries in a timely manner.
• Willingness to travel as required, approximately 60%.
• Legal right to work in the country where the role is based.

Nice To Haves

• Experience monitoring ophthalmology trials or trials across multiple therapeutic areas.

Responsibilities

• Coordinate activities for study setup and monitoring independently and proactively.
• Complete accurate study status reports and maintain study documentation.
• Efficiently manage sponsor-generated queries and take responsibility for study cost efficiency.
• Participate in preparing and reviewing study documentation and feasibility studies for new proposals as needed.
• Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Support patient safety by ensuring compliance with ICON procedures, study protocols, and regulatory requirements.

Benefits

• Competitive base salary and performance-related incentives.
• Medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Structured training and career development opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level