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Volunteer Icon Clinical Research Jobs (NOW HIRING)

Clinical Research Coordinator Level 1

Statesville, NC ยท On-site

$22.75 - $30.50/hr

We have an incredible opportunity for a Clinical Research Coordinator 1 to join ICON's Accellacare team. The CRC ensures the safety of our volunteers, promotes the mission of Accellacare, and strives ...

Clinical Research Coordinator Level 1

Piedmont, CA ยท On-site

$27.50 - $36.50/hr

We have an incredible opportunity for a Clinical Research Coordinator 1 to join ICON's Accellacare team. The CRC ensures the safety of our volunteers, promotes the mission of Accellacare, and strives ...

Patient Recruitment Associate ICON is a global healthcare intelligence and clinical research ... Identify appropriate study opportunities for interested volunteers based on knowledge of clinical ...

New

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key ... Identify appropriate study opportunities for interested volunteers based on knowledge of clinical ...

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key ... Identify appropriate study opportunities for interested volunteers based on knowledge of clinical ...

Clinical Research Coordinator

Johns Creek, GA ยท On-site

$22.50 - $30/hr

Clinical Research Coordinator 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 ...

Clinical Research Coordinator

Johns Creek, GA ยท On-site

$22.50 - $30/hr

Clinical Research Coordinator 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 ...

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site ...

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

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 ...

Clinical Research Nurse ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. We are currently ...

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Volunteer Icon Clinical Research information

See salary details

$15

$28

$42

How much do volunteer icon clinical research jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for volunteer icon clinical research in the United States is $28.69, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.01 per hour, depending on experience, location, and employer.

What is the difference between Volunteer Icon Clinical Research vs Clinical Research Coordinator?

AspectVolunteer Icon Clinical ResearchClinical Research Coordinator
CredentialsTypically no formal credentials required; some knowledge of clinical trialsOften requires a bachelor's degree in health sciences or related field; certification preferred
Work EnvironmentVolunteer settings, research sites, hospitalsResearch sites, hospitals, clinics
Employer & IndustryNon-profit organizations, research institutions, pharmaceutical companiesHospitals, research organizations, pharmaceutical companies
Search & Comparison IntentUnderstanding volunteer roles in clinical researchExploring professional roles and responsibilities in clinical trials

Volunteer Icon Clinical Research roles are typically volunteer-based with minimal formal credentials, focusing on assisting research activities. Clinical Research Coordinators are paid professionals with relevant education and certifications, responsible for managing clinical trial processes. Both work in research environments but differ mainly in qualifications and employment status.

What can I expect from the onboarding process as a volunteer in clinical research at ICON?

As a volunteer at Icon Clinical Research, the onboarding process typically involves an initial screening to assess eligibility, followed by a comprehensive orientation about the study's requirements and procedures. You will receive detailed information on your rights, potential risks, confidentiality, and the study timeline. The medical team will guide you through informed consent and answer any questions to ensure you are comfortable before participation. Throughout the study, you will collaborate closely with research staff and may need to attend scheduled visits for assessments or sample collections.

What are the key skills and qualifications needed to thrive as a volunteer in clinical research at ICON?

To thrive as a Volunteer in Clinical Research at ICON, you generally need to meet basic eligibility criteria such as good health, reliability, and clear communication skills, with no specific formal qualifications required. Familiarity with study protocols, informed consent procedures, and adherence to clinical trial guidelines is important, though most technical training is provided by the research team. Dependability, attention to detail, and the ability to follow instructions are valuable soft skills for this role. These qualities ensure the integrity of study data, participant safety, and the overall success of the research process.

Do volunteer icon clinical research volunteers get paid?

Volunteer icon clinical research roles are typically unpaid, as volunteers participate to support research efforts without compensation. However, some research studies may provide stipends or reimbursements for expenses like travel or time, depending on the study's design and sponsor policies.

What is a volunteer in clinical research at ICON?

Volunteer Icon Clinical Research roles typically involve participating in clinical trials as a volunteer at Icon, a global clinical research organization. Volunteers help advance medical science by testing new drugs, treatments, or medical devices under carefully controlled conditions. These roles are crucial for ensuring that new therapies are safe and effective before they become widely available to the public. Volunteers may be compensated for their time and travel, and their participation directly contributes to the development of future medical treatments.
More about Volunteer Icon Clinical Research jobs
What cities are hiring for Volunteer Icon Clinical Research jobs? Cities with the most Volunteer 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 Volunteer Icon Clinical Research jobs? States with the most job openings for Volunteer Icon Clinical Research jobs include:
Infographic showing various Volunteer Icon Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $59,666 per year, or $28.7 per hour.

Clinical Research Nurse I

ICON Clinical Research

San Antonio, TX โ€ข On-site

Other

Medical, Life, Retirement, PTO

Re-posted 11 days ago


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