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Volunteer Icon Clinical Research Jobs (NOW HIRING)

Senior Clinical Research Associate- Northeast ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Clinical Research Associate 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 ...

Senior Clinical Research Associate - Oncology - Knoxville, TN ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Senior Clinical Research Associate

Los Angeles, CA ยท On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Senior Clinical Research Associate - Oncology Phase I - Miami, FL ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Senior Clinical Research Associate

Washington, DC ยท On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Senior Clinical Research Associate 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 ...

Senior Clinical Research Associate

Chicago, IL ยท On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Senior Clinical Research Associate 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 ...

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Senior Clinical Research Associate 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 ...

Showing results 41-60

Volunteer Icon Clinical Research information

See salary details

$15

$28

$42

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

As of Sep 1, 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 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.

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.

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.

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.

Senior Clinical Research Associate

Icon plc

Blue Bell, PA โ€ข Remote

Full-time

Medical, Dental, Vision, Life, Retirement

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Senior CRA

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 organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking a Contractor Senior Clinical Research Associate to join our diverse and dynamic team. This will be for a 6 month contract. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

  • Bachelor's degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role

  • Minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

  • Strong organizational and communication skills, with attention to detail.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license

#LI-Remote #LI-ZH1


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.

Are you a current ICON Employee? Please click here to apply