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

Wellstar Health System

RN Research Coordinator

Marietta, GA · On-site

$65K - $81K/yr

... with Research Assistants and other research staff. - Gathers appropriate source documentation ... Ensures clinical trial and sponsor-required training is completed. - Ensures that all training ...

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

Experience with EDC systems and clinical trial management software preferred. * CCRC/CCRP ... certification a plus. Why Join Denali Health: * Work with a mission-driven team advancing clinical ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

This position offers flexible scheduling while providing critical support to our clinical trial ... Coordinate with Principal Investigators, study coordinators, sponsors, and CROs * Assist with ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

$55.10 - $82.66/hr

This position offers flexible scheduling while providing critical support to our clinical trial ... Coordinate with Principal Investigators, study coordinators, sponsors, and CROs * Assist with ...

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Showing results 21-40

All JobsClinical Trial JobsClinical Trial Assistant JobsClinical Trial Assistant Jobs in Decatur, GA

Clinical Trial Assistant information

See Decatur, GA salary details

$11

$36

$67

How much do clinical trial assistant jobs pay per hour?

As of Sep 5, 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 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 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 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 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.

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.

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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, 18% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $76,493 per year, or $36.8 per hour.

Clinical Research Coordinator

No-Resistance Consulting Group

Atlanta, GA • On-site

$22.50 - $25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago

Job description

Job Location:

AHF Peachtree, Atlanta Georgia

Expected Start Date:

October

Company Description:

Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urgent care centers throughout the north and southeast. We focus on sample collection and testing trials for lab device manufacturers with the purpose of collecting data to support the device's 510(k) or emergency use approval by the FDA. Notably, the trials we have participated in have directly led to the FDA EUA approval of three separate COVID-19 PCR testing platforms.

No clinical trial experience is required. No Resistance will train the right candidate(s). Hours are Monday-Friday 8:30 am to 5:00 pm with no weekend requirements. Hours may depend on clinical trial and clinic hours. 

Job Description:

No Resistance is seeking motivated individuals to join our team! In this role, you'll play a pivotal part in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.

Job Duties:

  • Maintaining regulatory binders, inventory of study-specific and clinical supplies.
  • Recruiting, and enrolling study subjects.
  • Obtaining informed consent.
  • Collecting nasal swab samples.
  • Testing samples on investigational laboratory PCR analyzers.
  • Data collection and entry.
  • Query resolution.
  • Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.

Key Success Factors:

  • Ability to work independently.
  • Desire to work in a clinical environment with direct patient contact.
  • Genuine interest in research.
  • Timely in all communications.
  • Superior attention to detail.

While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply. This position offers an exceptional opportunity to earn a competitive income while gaining invaluable experience highly regarded by medical school admission committees.

Job Type: Full-time

Pay: $22.50-$25.00 per hour

Expected hours: 40 per week

Benefits:

  • 401(k)
  • Dental Insurance
  • Health Insurance
  • Paid time off
  • Vision Insurance

Schedule:

  • Monday to Friday

Work Location: In person

Apply