Clinical Research Associate

ICON plc • Blue Bell, FL

2d

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 supports a client’s cardiovascular and obesity trials and contributes to clinical trial monitoring activities, with responsibility for assigned deliverables and collaboration with others. The posting refers to the position as CRA II and states that the candidate must be located in South, TX, although the heading identifies Georgia.

The CRA conducts site qualification, initiation, monitoring, and close-out visits; ensures protocol compliance, data integrity, and patient safety; collaborates with investigators and site staff; reviews data and resolves queries; and contributes to preparing and reviewing study documentation, including protocols and clinical study reports. Travel is approximately 60% as required.

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%.
• Must have the legal right to work in the country where the role is based.
• Must be located in South, TX, as stated in the position description.

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.
• Take responsibility for deliverables and collaborate on clinical trial monitoring activities.

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