Clinical Research Associate

Regulatory Jobs; San Antonio (TX); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive salary and incentives

Health, dental & vision coverage

Retirement plans

Life insurance & disability

Employee assistance programs

Learning & career development

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II in Texas to monitor clinical trials, ensuring protocol adherence, data integrity, and patient safety. You will work with investigators and site staff to drive quality study conduct in a sponsor-dedicated environment.

The role requires a life sciences degree and at least 2 years of CRA experience, with travel up to 60% and the ability to work independently in a fast-paced setting.

Qualifications

• Bachelor's degree in a scientific or healthcare field.
• Minimum 2 years of CRA experience.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP.
• Strong organizational and communication skills.
• Willingness to travel approximately 60%.
• Legal right to work in the United States.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance, data integrity, and patient safety.
• Collaborate with investigators and site staff for smooth study conduct.
• Perform data review and resolve queries to maintain quality data.
• Contribute to study documentation review including protocols and CSRs.

Skills

CRA experience

ICH-GCP knowledge

Regulatory knowledge

Organizational skills

Communication skills

Travel readiness

Education

Bachelor's degree in life sciences

Job description

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.

What You Will Do

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.

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.