Clinical Reseach Associate I

ICON; United States; Remote; USD 65,000 - 90,000; Full time

Job summary

ICON is seeking a Clinical Research Associate to deliver high-standard monitoring for clinical trials, working closely with the team and stakeholders.

Responsibilities include coordinating setup and monitoring activities, producing accurate status reports, and maintaining study documentation. You will run sponsor queries, support cost efficiency, and assist with feasibility studies. Travel around 60% is required.

Qualifications

• University degree in medicine or science (or equivalent).
• At least 6 months of CRA experience; senior CTAs or experienced Study Coordinators may be considered.
• Excellent written and verbal English communication.
• Knowledge of ICH-GCP guidelines and ability to review medical data.

Responsibilities

• Coordinate all activities for setting up and monitoring a study, and complete accurate study status reports and documentation.
• Run sponsor-generated queries efficiently and support study cost efficiency; assist in study documentation and feasibility reviews for new proposals.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety and compliance with ICON procedures, protocols, and regulatory requirements.

Skills

CRA experience

English communication

ICH-GCP knowledge

stakeholder communication

travel readiness

Education

University degree in medicine/science

Job description

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
• At least 6 months of CRA experience ; can consider experienced Senior CTAs and/or experienced Study Coordinators.
• Excellent written and verbal communication in English
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Good social skills enabling you to deal with queries in a timely manner
• Willingness to travel as required (approximately 60%)

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here