Clinical Research Associate

Regulatory Jobs; Miami (FL); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programs

Retirement and pension plans

Life assurance and disability coverage

Training and career development

Job summary

ICON Strategic Solutions in Florida is seeking a Clinical Research Associate II to monitor trials and ensure data integrity and patient safety. You will manage site visits, review data, and collaborate with investigators to support cardio and obesity studies from a sponsor-dedicated model.

Ideal candidates have a scientific degree and 2+ years in CRA roles, with strong organizational skills and willingness to travel. Employment is contingent on work authorization in the U.S.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Experience in monitoring clinical trials and ensuring patient safety.
• Solid knowledge of ICH-GCP guidelines and regulatory requirements.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance, data integrity and patient safety.
• Collaborate with investigators and site staff to support study conduct.
• Perform data review and resolve queries for high-quality data.
• Assist in preparing study documentation including protocols and reports.

Skills

Clinical trial monitoring

ICH-GCP guidelines

Data review and queries

Communication

Travel readiness

Education

Bachelor's degree in a scientific or healthcare field

Job description

Clinical Research Associate - Florida

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This position is sponsor dedicated supporting our client monitoring cardio and obesity trials. Must be located in Miami, FL.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

• 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

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

• 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%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.