Clinical Research Associate
- Location
- Florida · On-site
- Job type
- Full-time
- Level
- Senior
- Experience
- 2+ years
- Education
- Bachelor's degree
- Listed
- 18 days ago
Skills & highlights for this role
- Clinical trial monitoring
- Site qualification, initiation, monitoring, and close-out
- ICH-GCP guidelines
- Clinical trial processes and regulations
- Data review and query resolution
- Organizational skills
- Communication skills
- Attention to detail
Also useful
- Cardiovascular trial experience
- Obesity trial experience
- Protocol and clinical study report authoring
About the role
Clinical Research Associate - Texas 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 South, TX.
Pay and benefits
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: 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.
Required qualifications and experience: 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. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. Are you a current ICON Employee? Please click here to apply
Equal opportunity and legal notices
Inclusion and Accessibility ICON is an equal opportunity employer. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
From ICON's careers page, first listed on Rolev.ai on October 23, 2026. Rolev.ai is not the employer.
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More at ICON
All ICON jobsCommon questions
Where is the Clinical Research Associate job at ICON located?
This Clinical Research Associate position at ICON is located in Florida (On-site). Always check ICON's application page for specific state eligibility or relocation policies.
What qualifications are required for Clinical Research Associate at ICON?
For the Clinical Research Associate role, ICON highlights 2+ years of relevant experience; a bachelor's degree; experience with Clinical trial monitoring, Site qualification, initiation, monitoring, and close-out, ICH-GCP guidelines, Clinical trial processes and regulations, Data review and query resolution, Organizational skills. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.
How do I apply for the Clinical Research Associate position at ICON?
This listing links directly to ICON's Workday application page. You can apply directly on ICON's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.