Clinical Research Associate II: Monitoring & Data Quality

Regulatory Jobs; Texas; Hybrid; USD 70,000 - 95,000; Full time

Benefits offered by this job

Competitive base salary

Health coverage

Retirement plans

Life insurance

Employee assistance programs

Learning and development opportunities

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II for the South Central/Texas region. You will design and analyze clinical trials, monitor sites, ensure data integrity, and support study documentation, contributing to treatments that benefit patients globally.

Ideal candidates have a minimum of two years as a CRA, solid knowledge of trial regulations, and strong organizational and communication skills, with travel about 60% expected.

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 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 trial monitoring

ICH-GCP knowledge

Organizational skills

Communication skills

Willingness to travel

Education

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

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II for the South Central/Texas region. You will design and analyze clinical trials, monitor sites, ensure data integrity, and support study documentation, contributing to treatments that benefit patients globally.

Ideal candidates have a minimum of two years as a CRA, solid knowledge of trial regulations, and strong organizational and communication skills, with travel about 60% expected.