CRA II: Cardio & Obesity Trials (Sponsor-Dedicated)

Regulatory Jobs; Florida; On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Salary and incentive rewards

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Wellbeing resources

Structured training and career paths

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to join our sponsor-dedicated team. You will design and monitor trials, ensuring data integrity and patient safety while collaborating with investigators and site staff. This role supports cardio and obesity trials and requires travel approximately 60%.

The position emphasizes independent work in a fast-paced environment and adherence to ICH-GCP guidelines. Employment is contingent on eligibility to work in the United States.

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.

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

Attention to detail

Strong communication

Independent work

Education

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

Tools

ICH-GCP knowledge

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II to join our sponsor-dedicated team. You will design and monitor trials, ensuring data integrity and patient safety while collaborating with investigators and site staff. This role supports cardio and obesity trials and requires travel approximately 60%.

The position emphasizes independent work in a fast-paced environment and adherence to ICH-GCP guidelines. Employment is contingent on eligibility to work in the United States.