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Clinical Trial Assistant Jobs in Decatur, GA (NOW HIRING)

ICON

Clinical Research Coordinator

Johns Creek, GA · On-site

$22.50 - $30/hr

Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes. * Managing study-related documentation ...

Icon plc

Clinical Research Coordinator

Johns Creek, GA · On-site

$22.50 - $30/hr

Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes. * Managing study-related documentation ...

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

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.

UCB

Senior Principal Programmer, Atlanta, GA

Atlanta, GA · Hybrid

What you'll do You will review and coordinate clinical trial analysis and reporting setup requests ... Should you require any adjustments to our process to assist you in demonstrating your strengths and ...

UCB

Senior Principal Programmer, Atlanta, GA

Atlanta, GA · On-site

What you'll do You will review and coordinate clinical trial analysis and reporting setup requests ... Should you require any adjustments to our process to assist you in demonstrating your strengths and ...

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Clinical Trial Assistant information

See Decatur, GA salary details

$11

$36

$67

How much do clinical trial assistant jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical trial assistant in Decatur, GA is $36.78, according to ZipRecruiter salary data. Most workers in this role earn between $25.10 and $46.92 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trial assistant?

To thrive as a Clinical Trial Assistant, you need a solid understanding of clinical research processes, attention to detail, and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, trial management software, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Strong organizational skills, effective communication, and the ability to multitask help you excel in supporting clinical trial operations. These skills ensure protocol compliance, data accuracy, and smooth coordination within clinical research teams.

What does a clinical trial assistant do?

A clinical trial assistant is responsible for monitoring the medical and administrative procedures during a clinical trial. In this career, you prepare patients for tests, take blood, perform laboratory work, prep for medical treatments, and collect data for research. You work with project managers and research associates throughout the beginning, implementation, and closeout of the trial. You also handle paperwork, file records, prepare reports, label medication, track progress, and fulfill other duties that arise during medical studies. You may assist with appointment schedules, plan meetings, and communicate with external sources and investigators as well.

What is the difference between Clinical Trial Assistant vs Clinical Research Coordinator?

AspectClinical Trial AssistantClinical Research Coordinator
ResponsibilitiesSupports trial logistics, manages documentation, assists with regulatory complianceOversees study conduct, recruits participants, manages site operations
CredentialsTypically requires a bachelor's degree in health or life sciencesOften requires a bachelor's or master's degree in health sciences or related fields
Work EnvironmentResearch sites, sponsor offices, clinical trial centersClinical sites, hospitals, research institutions
Industry UsageCommonly employed in pharmaceutical companies, CROs, research institutionsPrimarily in hospitals, clinics, research centers

The Clinical Trial Assistant primarily supports trial logistics and documentation, working closely with the research team. In contrast, the Clinical Research Coordinator manages the overall conduct of the study, including participant recruitment and site management. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What is a clinical trial assistant?

Clinical Trial Assistants (CTAs) are professionals who provide administrative support to clinical research teams during the planning, execution, and close-out of clinical trials. They help ensure that studies comply with regulatory standards, maintain accurate documentation, and coordinate communication between different stakeholders. CTAs often manage trial master files, track study progress, and assist with scheduling meetings and site visits. Their work is essential to the smooth operation of clinical studies and the integrity of collected data.

What are some typical challenges a clinical trial assistant may face when supporting multiple trials simultaneously?

Clinical Trial Assistants often support several studies at once, which can make time management and organization challenging. Balancing competing priorities, meeting tight regulatory deadlines, and ensuring accurate documentation are common hurdles. Effective communication with study coordinators, principal investigators, and sponsors is essential to keep all parties informed and processes running smoothly. Proactively using organizational tools and regularly updating tracking systems can help manage this fast-paced environment.
More about Clinical Trial Assistant jobs
What are the most commonly searched types of Clinical Trial jobs in Decatur, GA? The most popular types of Clinical Trial jobs in Decatur, GA are:
What are popular job titles related to Clinical Trial Assistant jobs in Decatur, GA? For Clinical Trial Assistant jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Assistant jobs in Decatur, GA look for? The top searched job categories for Clinical Trial Assistant jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Trial Assistant jobs? Cities near Decatur, GA with the most Clinical Trial Assistant job openings:
Clinical Trial Assistant jobs near you
Infographic showing various Clinical Trial Assistant job openings in Decatur, GA as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 16% Part Time, 2% Temporary, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $76,493 per year, or $36.8 per hour.

Clinical Research Coordinator

ICON

Johns Creek, GA • On-site

$22.50 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.

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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