Clinical Research Associate 2

ICON plc • Blue Bell, MO

5d

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 monitoring activities, takes responsibility for deliverables, and works collaboratively. It involves designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of treatments and therapies.

Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• At least 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required, approximately 60%.
• Legal right to work in the country where the role is based.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolve queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

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: Mid Level