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Icon Clinical Research Jobs (NOW HIRING)

Clinical Research Administrator

Lisle, IL

$38K - $48K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

New

Clinical Research Administrator

Oak Lawn, IL

$38K - $48K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

New

Clinical Research Administrator

Lombard, IL · On-site

$38K - $48K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

New

Clinical Research Administrator

Winfield, IL · On-site

$38K - $48K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

New

Clinical Research Administrator

Downers Grove, IL · On-site

$38K - $48K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

New

Clinical Research Coordinator Level 1

Piedmont, CA · On-site

$27.50 - $36.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Coordinator Level 1 - Statesville, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Clinical Research Coordinator Level 1

Statesville, NC · On-site

$22.75 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Coordinator Level 1 - Statesville, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Medical Monitor

Lenexa, KS · On-site

  • Medical

  • Life

  • Retirement

  • PTO

Medical Monitor ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we ...

Senior Clinical Research Associate

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior CRA/ CRA II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Medical Supply Kit Production Associate

Blue Bell, PA · On-site

$14.25 - $18.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Medical Supply Kit Production Associate - Blue Bell, PA (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

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Showing results 1-20

Icon Clinical Research information

See salary details

$49K

$107.3K

$189K

How much do icon clinical research jobs pay per year?

As of Aug 13, 2026, the average yearly pay for icon clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Icon Clinical Research position, and why are they important?

To thrive at ICON Clinical Research, you typically need a background in life sciences or a related field, experience with clinical trial processes, and strong analytical skills. Familiarity with industry-standard clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are highly valued. Excellent organizational skills, attention to detail, and effective communication help you excel in a collaborative research environment. These skills are crucial to ensure regulatory compliance, data integrity, and successful execution of clinical trials.

What does a typical day look like for someone working at Icon Clinical Research?

A typical day at ICON Clinical Research often involves collaborating with cross-functional teams to oversee the progress of clinical trials, monitoring study data for accuracy, and ensuring all activities adhere to regulatory standards. You'll attend project meetings, communicate regularly with sponsors and investigators, and manage documentation and reporting tasks using specialized software. Depending on your specific role, you may also be responsible for site management, participant enrollment, or clinical data review. The work environment is fast-paced and supportive, offering opportunities for professional growth and advancement within the clinical research field.

What is an Icon Clinical Research?

An ICON Clinical Research job typically involves working for ICON plc, a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. Roles at ICON can range from clinical research associates and project managers to data analysts and regulatory specialists. Employees help design, manage, and monitor clinical trials to ensure they meet regulatory and ethical standards. These positions often require experience in clinical research, strong attention to detail, and adherence to Good Clinical Practice (GCP) guidelines.

What cities are hiring for Icon Clinical Research jobs?

Cities with the most Icon Clinical Research job openings:

What are the most commonly searched types of Icon Clinical Research jobs?

The most popular types of Icon Clinical Research jobs are:

What states have the most Icon Clinical Research jobs?

States with the most job openings for Icon Clinical Research jobs include:

Infographic showing various Icon Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Nurse I

ICON Clinical Research

San Antonio, TX • On-site

Other

Medical, Life, Retirement, PTO

This job post has expired 4 days ago. Applications are no longer accepted.


Job description

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Research Nurse I to join our diverse and dynamic team. As a Clinical Research Nurse I at ICON, you will play a pivotal role in supporting the execution of clinical trials, ensuring adherence to protocol requirements, and providing compassionate patient care throughout the research process.

Location: 100% on site- San Antonio TX 78209

Job Type : PRN / As Needed

Shift/Schedule : M-F 6 AM-2:30 PM

What you will be doing:

  • Assisting in the planning, implementation, and coordination of clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures (SOPs).

  • Conducting patient assessments, administering study treatments, and performing clinical procedures as required by the research protocol, while ensuring patient safety and compliance with ethical standards.

  • Collecting, recording, and maintaining accurate and complete data documentation, including medical histories, vital signs, adverse events, and laboratory results, in electronic case report forms (eCRFs) and study databases.

  • Collaborating with multidisciplinary teams, including investigators, study coordinators, and regulatory staff, to ensure efficient study conduct, participant recruitment, and retention throughout the duration of the trial.

  • Providing education and counseling to study participants and their families regarding study procedures, treatment regimens, and informed consent, while addressing any questions or concerns that may arise during the course of the study.

Your profile:

  • Must hold a current and valid Registered Nurse (RN) license in the state of Texas.

  • Minimum of 1-2 years of clinical nursing experience, preferably in a research or academic healthcare setting, with exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines.

  • Strong clinical assessment and critical thinking skills, with the ability to recognize and respond to changes in patient status and communicate effectively with healthcare professionals and study investigators.

  • Knowledge of regulatory requirements governing clinical research, including the International Council for Harmonization (ICH) guidelines and local regulatory requirements, with a commitment to upholding ethical standards and patient confidentiality.

  • Proficiency in electronic medical record (EMR) systems, clinical documentation, and data entry, with a high level of attention to detail and accuracy in recording patient information and study data.

  • Excellent interpersonal and organizational skills, with the ability to work independently and collaboratively in a fast-paced, multidisciplinary environment, while prioritizing competing demands and meeting project deadlines.

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 (https://careers.iconplc.com/benefits) 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 (https://careers.iconplc.com/reasonable-accommodations)

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply