Clinical Research Associate II — Cardio & Obesity Trials

Regulatory Jobs; Texas; On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Competitive salary and incentives

Health and wellbeing programs

Retirement plans

Life assurance and disability coverage

Employee assistance programs

Structured training and career paths

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate to monitor trials and support cardio and obesity studies. The role requires site visits, data integrity, and collaboration with investigators. A science/healthcare degree and 2+ years of CRA experience are expected, with travel about 60% of the time.

This sponsor-dedicated position contributes to advancing therapies and patient care. Applicants should be prepared to work in a fast-paced environment and ensure quality data and

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 travel 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 study conduct.
• Perform data review and resolve queries to maintain high-quality clinical data.
• Contribute to preparation and review of study documentation, including protocols and reports.

Skills

Clinical trial monitoring

Data integrity

Regulatory compliance

ICH-GCP knowledge

Communication

Organization

Education

Bachelor's degree in science or healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate to monitor trials and support cardio and obesity studies. The role requires site visits, data integrity, and collaboration with investigators. A science/healthcare degree and 2+ years of CRA experience are expected, with travel about 60% of the time.

This sponsor-dedicated position contributes to advancing therapies and patient care. Applicants should be prepared to work in a fast-paced environment and ensure quality data and