Clinical Research Associate

ICON plc • Blue Bell, OR

6d • $91,336 - $114,170

About The Position

At ICON Strategic Solutions, the Clinical Research Associate works in a sponsor-dedicated model, supported by ICON’s global expertise. The role contributes to clinical trial operations and collaborates with teams and stakeholders to deliver high-quality outcomes across clinical programmes. It involves coordinating study set-up and monitoring, maintaining accurate study records and reports, supporting study documentation and feasibility work, and promoting patient safety and regulatory compliance. Travel is required as needed, approximately 60%.

Requirements

• University degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines.
• Expertise in reviewing and evaluating medical data.
• Excellent written and verbal communication skills in English.
• Good social skills to address queries in a timely manner.
• Willingness to travel as required, approximately 60%.

Responsibilities

• Coordinate activities for study set-up and monitoring independently and proactively.
• Complete accurate study status reports and maintain study documentation.
• Run sponsor-generated queries efficiently and take responsibility for study cost efficiency.
• Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.
• Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety and compliance with ICON procedures, 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.
• Learning and development opportunities through structured training and career pathways.

What This Job Offers

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