Clinical Research Associate

ICON plc • Blue Bell, IN

6d • $91,336 - $114,170

About The Position

The Clinical Research Associate will work in a sponsor-dedicated model at ICON Strategic Solutions, contributing to clinical trial operations and collaborating with teams and stakeholders to deliver high-quality outcomes across clinical programmes. The role involves clinical trial monitoring and coordinating study setup and monitoring activities. The position covers the Central/Mid-West region and requires approximately 60% travel.

Requirements

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

Responsibilities

• Independently coordinate activities for setting up and monitoring a study.
• 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 required.
• Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Help ensure patient safety by complying 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