Clinical Research Associate

Regulatory Jobs; Texas; On-site; USD 80,000 - 110,000; Full time

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate in Texas/South Central. You will deliver monitoring work within a sponsor-dedicated model, ensuring patient safety and regulatory compliance.

The role emphasizes building strong relationships with investigators and site staff while coordinating study setup and monitoring activities. The candidate should have an university degree in medicine or science, strong English communication, and willingness to travel up to 60%.

Qualifications

• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Good social skills enabling you to deal with queries in a timely manner.
• Willingness to travel as required (approximately 60%).

Responsibilities

• Deliver clinical trial monitoring work to a high standard.
• Coordinate all activities for setting up and monitoring a study and maintain study documentation.
• Run sponsor generated queries efficiently and support cost efficiency; assist in feasibility studies for new proposals.
• Develop and maintain strong relationships with stakeholders, clinical investigators, and site staff.
• Ensure patient safety by complying with ICON's procedures, protocols, and regulatory requirements.

Skills

ICH-GCP knowledge

English communication

Social skills

Willingness to travel

Education

University degree in medicine/science

Job description

Clinical Research Associate - Texas/South Central

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.

What You Will Do

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Your Profile

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

Required qualifications and experience:

• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills enabling you to deal with queries in a timely manner
• 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.