Clinical Research Associate

Regulatory Jobs; Chicago (IL); On-site; USD 91,000 - 114,000; Full time

Job summary

ICON Strategic Solutions in Chicago is seeking a Clinical Research Associate (CRA I) to perform high-standard clinical trial monitoring within a sponsor-dedicated model. You will coordinate activities, maintain documentation, and ensure patient safety while collaborating with investigators and site staff.

The role requires 60% travel, strong knowledge of ICH-GCP, and excellent English communication. Employment is contingent on legal work authorization in the U.S.

Qualifications

• 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%).

Responsibilities

• Coordinate study setup and monitoring with independence; produce accurate status reports and maintain study documentation.
• Manage sponsor-generated queries and support study cost efficiency; assist in feasibility and proposals as needed.
• Develop and maintain strong relationships with clinical investigators and site staff.
• Ensure patient safety by complying with ICON procedures, protocols, and regulatory requirements.

Skills

Degree in medicine/science

ICH-GCP knowledge

English communication

Social skills

Travel willingness

Education

University degree in medicine/science

Job description

Clinical Research Associate- Central/Mid-West

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 I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

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.

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 requesthere.

Salary Range

$91,336.00-$114,170.00