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Volunteer Icon Clinical Research Jobs in Decatur, GA

ICON

Clinical Research Coordinator

Johns Creek, GA · 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 ...

Icon plc

Clinical Research Coordinator

Johns Creek, GA

$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 ...

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Icon plc

Senior CRA

Atlanta, GA

Sr CRA - Oncology - GA FL - Astellas 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 ...

Syneos Health

CRC II (Onsite) - Marietta, GA

Marietta, GA · On-site

$23 - $30.50/hr

Job Responsibilities Clinical Research Project Planning and Preparation * Review of assigned ... Finalize study and/or volunteer logs. * Ensure completion of other close-out activities as required ...

Breakthrough T1D

Development Manager

Atlanta, GA · Hybrid

Partner with volunteer leadership to solicit funding and other support from individuals ... research, advocacy, and community engagement and clinical trials. * Represent the interests ...

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Volunteer Icon Clinical Research information

See Decatur, GA salary details

$15

$28

$41

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

As of Jul 31, 2026, the average hourly pay for volunteer icon clinical research in Decatur, GA is $28.01, according to ZipRecruiter salary data. Most workers in this role earn between $22.79 and $30.29 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 Icon Clinical Research studies?

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, and why are they important?

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 are Volunteer Icon Clinical Research roles?

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 are popular job titles related to Volunteer Icon Clinical Research jobs in Decatur, GA? For Volunteer Icon Clinical Research jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Volunteer Icon Clinical Research jobs in Decatur, GA look for? The top searched job categories for Volunteer Icon Clinical Research jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Volunteer Icon Clinical Research jobs? Cities near Decatur, GA with the most Volunteer Icon Clinical Research job openings:
Volunteer Icon Clinical Research jobs near you

Clinical Research Coordinator

ICON

Johns Creek, GA • On-site

$22.50 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 17 days ago

Job description

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-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Shift: 10:30 AM - 7:00 PM, Monday to Friday (8 working hours with a 30-minute unpaid lunch break), with flexibility required. The role will include at least two Saturdays per month, with Saturday shifts scheduled from 8:00 AM - 4:00 PM. A weekday off will be provided in lieu of each Saturday worked.
What You Will Do:
Your role will involve delivering clinical coordination work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
  • Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
  • Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
  • Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
  • Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
  • Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.

Your Profile:
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required qualifications and experience:
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
  • Previous experience working in clinical research or healthcare settings preferred.
  • Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
  • Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
  • Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.

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

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