CRA II for Cardio & Obesity Trials | 60% Travel

ICON

Florida

On-site

USD 70,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Annual leave entitlements
Health insurance offerings
Competitive retirement planning
Global Employee Assistance Programme (
Life assurance
Country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II in Florida. You will design and monitor clinical trials in a sponsor-dedicated model, contributing to cardio and obesity studies.

The role requires travel around 60% and collaboration with investigators to ensure safety, data integrity, and protocol adherence. Ideal candidates hold a science degree, at least 2 years as a CRA, and thorough knowledge of ICH-GCP guidelines.

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.
  • Willingness 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 smooth study conduct.
  • Perform data review and resolution of queries to maintain high-quality clinical data.
  • Contribute to preparation and review of study documentation, including protocols and final study reports.

Skills

Clinical trial monitoring
ICH-GCP knowledge
Data review
Travel readiness

Education

Bachelor's degree in science

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II in Florida. You will design and monitor clinical trials in a sponsor-dedicated model, contributing to cardio and obesity studies.

The role requires travel around 60% and collaboration with investigators to ensure safety, data integrity, and protocol adherence. Ideal candidates hold a science degree, at least 2 years as a CRA, and thorough knowledge of ICH-GCP guidelines.

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