Clinical Research Associate - Monitor Trials & Data Integrity

ICON Strategic Solutions; Boston (MA); On-site; USD 75,000 - 120,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Life insurance

Employee assistance programs

Job summary

ICON is a global healthcare intelligence and clinical research organization focused on speeding the delivery of new medicines and treatments. As a CRA at ICON, you will design and analyze clinical trials, interpreting complex medical data and contributing to innovative therapies.

You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Travel about 60% is expected.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with understanding of clinical trial processes and regulatory requirements.
• Ability to manage multiple sites and projects simultaneously with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills with ability to influence and drive compliance within a complex environment.
• Willingness to travel to sites approximately 60% of the time.

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Skills

Clinical trial monitoring

Site management

Data integrity

Regulatory compliance

Communication

Stakeholder management

Travel readiness

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Tools

Clinical trial software

Job description

ICON is a global healthcare intelligence and clinical research organization focused on speeding the delivery of new medicines and treatments. As a CRA at ICON, you will design and analyze clinical trials, interpreting complex medical data and contributing to innovative therapies.

You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Travel about 60% is expected.