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Volunteer Icon Clinical Research Jobs in Decatur, GA

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 Clinical Research Associate

Atlanta, GA · On-site

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 · On-site

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 ...

Actalent

Clinical Research Coordinator

Atlanta, GA · On-site

$22 - $25/hr

Clinical Research Coordinator The Clinical Research Coordinator will support a post-market ... Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term ...

New

Actalent

Clinical Research Coordinator

Atlanta, GA

$22 - $25/hr

Clinical Research Coordinator The Clinical Research Coordinator will support a post-market ... Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term ...

New

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 ...

Cox Automotive

UX Designer II

Dunwoody, GA · On-site

$98K - $147K/yr

... research. You'll contribute to design critiques, collaborate on user testing, and help refine our ... Extend and apply the design system using reusable components, icon libraries, templates, and brand ...

Cox Automotive

UX Designer II

Atlanta, GA · On-site

$98K - $147K/yr

... research. You'll contribute to design critiques, collaborate on user testing, and help refine our ... Extend and apply the design system using reusable components, icon libraries, templates, and brand ...

Cox Automotive

UX Designer II

Decatur, GA · On-site

$98K - $147K/yr

... research. You'll contribute to design critiques, collaborate on user testing, and help refine our ... Extend and apply the design system using reusable components, icon libraries, templates, and brand ...

Cox Automotive

UX Designer II

Brookhaven, GA · On-site

$98K - $147K/yr

... research. You'll contribute to design critiques, collaborate on user testing, and help refine our ... Extend and apply the design system using reusable components, icon libraries, templates, and brand ...

Cox Automotive

UX Designer II

Peachtree Corners, GA · On-site

$98K - $147K/yr

... research. You'll contribute to design critiques, collaborate on user testing, and help refine our ... Extend and apply the design system using reusable components, icon libraries, templates, and brand ...

Cox Automotive

UX Designer II

Chamblee, GA · On-site

$98K - $147K/yr

... research. You'll contribute to design critiques, collaborate on user testing, and help refine our ... Extend and apply the design system using reusable components, icon libraries, templates, and brand ...

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All JobsVolunteer Icon Clinical Research JobsVolunteer Icon Clinical Research Jobs in Decatur, GA

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 Aug 20, 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 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.

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Volunteer Icon Clinical Research jobs near you

Senior Clinical Research Associate

ICON

Atlanta, GA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 19 days ago

Job description

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 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.
To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib.
  • The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered.

3 years of monitoring experience required.
A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
Candidates must have/ be:
  • In-depth knowledge of FDA regulations and ICH/GCP guidelines.
  • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
  • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
  • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
  • Ability to work independently and manage multiple priorities in a dynamic environment.
  • A well-executed plan for communication with the study teams and sites.
  • Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports.
  • Located in the US near a major airport. Ability to cover up to 65% regional travel.

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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