Clinical Research Associate II — West Coast Trial Monitoring & Data

ICON plc; Nevada; On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning options

Global Employee Assistance Programme

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to support West Coast trials in a sponsor-dedicated model. You will design and analyze trials, ensure compliance and data integrity, and collaborate with investigators to advance therapies.

Travel up to ~60% is required; strong organization and communication are essential as you monitor sites, perform qualification and close-out visits, and review 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

• 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

Site monitoring

Clinical data review

ICH-GCP knowledge

Regulatory knowledge

Travel readiness

Communication skills

Organizational skills

Education

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

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II to support West Coast trials in a sponsor-dedicated model. You will design and analyze trials, ensure compliance and data integrity, and collaborate with investigators to advance therapies.

Travel up to ~60% is required; strong organization and communication are essential as you monitor sites, perform qualification and close-out visits, and review study documentation.