Traveling Clinical Research Associate - Impactful Trials

ICON Strategic Solutions; Los Angeles (CA); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Competitive base salary

Health coverage

Career development

Job summary

ICON Strategic Solutions in Los Angeles is seeking a Clinical Research Associate to support site qualification, initiation, monitoring, and close-out visits across clinical trials. You will ensure protocol compliance and data integrity, collaborate with investigators, and review study documentation while traveling about 60% of the time.

A Bachelor's in science and 2+ years CRA experience are required. ICON offers a competitive base salary, comprehensive benefits, and opportunities for career

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

• 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 monitoring

ICH-GCP

Data integrity

Travel readiness

Communication

Documentation

Education

Bachelor's in science

Job description

ICON Strategic Solutions in Los Angeles is seeking a Clinical Research Associate to support site qualification, initiation, monitoring, and close-out visits across clinical trials. You will ensure protocol compliance and data integrity, collaborate with investigators, and review study documentation while traveling about 60% of the time.

A Bachelor's in science and 2+ years CRA experience are required. ICON offers a competitive base salary, comprehensive benefits, and opportunities for career