Senior CRA — Sponsor-Dedicated Trials (60% Travel)

ICON Strategic Solutions; Nashville (TN); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Life assurance

Employee assistance programmes

Training and career pathways

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate to work in a sponsor-dedicated model with global support. You will conduct site qualification, initiation, monitoring, and close-out visits across multiple therapeutic areas, ensuring data integrity and patient safety.

The role requires collaboration with investigators and site staff, thorough data review, and preparation of study documentation.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 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%)

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 resolution of queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Skills

Bachelor's degree

CRA experience

ICH-GCP knowledge

Regulatory knowledge

Travel 60%

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate to work in a sponsor-dedicated model with global support. You will conduct site qualification, initiation, monitoring, and close-out visits across multiple therapeutic areas, ensuring data integrity and patient safety.

The role requires collaboration with investigators and site staff, thorough data review, and preparation of study documentation.