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

NP/PA, Phase One Clinical Trials

Atlanta, GA · On-site

$106K - $137K/yr

Our Physician Assistants and Nurse Practitioners are an integral part of the Emory Healthcare ... Comprehensive health benefits that start Day 1 Our Winship Clinical Trials team is growing and we ...

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How much do clinical trials assistant jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for clinical trials assistant in Decatur, GA is $19.75, according to ZipRecruiter salary data. Most workers in this role earn between $16.20 and $22.79 per hour, depending on experience, location, and employer.

What are Clinical Trials Assistants?

Clinical Trials Assistants (CTAs) are professionals who support the planning, coordination, and administration of clinical trials, which are research studies that evaluate the safety and effectiveness of medical treatments or interventions. They handle tasks such as maintaining trial documentation, assisting with regulatory submissions, scheduling meetings, and ensuring data accuracy. CTAs play a crucial role in helping clinical research teams comply with protocols and regulatory requirements, making the clinical trial process run smoothly and efficiently.

What are some typical challenges a Clinical Trials Assistant faces during a study, and how can they be managed?

Clinical Trials Assistants often encounter challenges such as managing large volumes of documentation, ensuring timely data entry, and coordinating communication among multiple stakeholders. Staying organized and using established tracking systems can help manage documents efficiently. Proactive communication and regular check-ins with team members—such as study coordinators and data managers—are key to resolving issues quickly and maintaining study timelines. Embracing good time management practices and seeking mentorship from senior staff can further ease these common challenges.

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

AspectClinical Trials AssistantClinical Research Coordinator
CredentialsHigh school diploma or equivalent; some roles may require certificationBachelor’s degree in health sciences or related field; often requires certification
Work EnvironmentResearch sites, hospitals, clinics, pharmaceutical companiesResearch sites, hospitals, clinics, pharmaceutical companies
ResponsibilitiesAssist with data entry, document management, and trial logisticsOversee trial processes, patient recruitment, data collection, and compliance
Industry UsageCommonly used in clinical trial support rolesMore involved in trial management and coordination

While both roles support clinical trials, Clinical Trials Assistants focus on administrative and logistical tasks, whereas Clinical Research Coordinators handle more comprehensive trial management, patient interactions, and compliance activities.

What are the key skills and qualifications needed to thrive as a Clinical Trials Assistant, and why are they important?

To thrive as a Clinical Trials Assistant, you need a solid understanding of clinical research processes, regulatory guidelines, and attention to detail, often supported by a degree in life sciences. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, effective communication, and the ability to multitask make candidates stand out in this role. These skills are essential for ensuring compliance, accurate documentation, and the smooth execution of clinical studies.
What are the most commonly searched types of Clinical Trials jobs in Decatur, GA? The most popular types of Clinical Trials jobs in Decatur, GA are:
What are popular job titles related to Clinical Trials Assistant jobs in Decatur, GA? For Clinical Trials Assistant jobs in Decatur, GA, the most frequently searched job titles are:
What cities near Decatur, GA are hiring for Clinical Trials Assistant jobs? Cities near Decatur, GA with the most Clinical Trials Assistant job openings:
Infographic showing various Clinical Trials Assistant job openings in Decatur, GA as of June 2026, with employment types broken down into 1% Locum Tenens, 68% Full Time, 19% Part Time, 1% Temporary, and 11% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $41,084 per year, or $19.8 per hour.
Clinical Trial Assistant

Clinical Trial Assistant

VIVEX BIOLOGICS INC

Atlanta, GA • On-site

Full-time

Posted 8 days ago


Job description

Description:

Job purpose

The Clinical Trial Assistant will provide administrative support to the Clinical team. Responsible for assisting with day-to-day operations of clinical studies. This position requires basic knowledge of clinical trials, excellent organizational skills and the ability to perform at high levels in a fast-paced, dynamic environment.

Duties and responsibilities

  1. Assist team members with designated administrative tasks in support of clinical trial execution and management.
  2. Perform study tracking to ensure that study files are current, accurate and complete with applicable local regulatory requirements and ICH/GCP guidelines.
  3. Assist in generation of study start up materials and support feasibility study activities.
  4. Participate in the design and implementation of case report forms (CRF) and completion guidelines, and database testing.
  5. Maintain clinical study schedules; collaborate with study team on subject tracking to ensure protocol compliance.
  6. Maintain and organize publication library, clinical study documents and reference materials.
  7. Assist Clinical Research Associates (CRA) and management with resolution of issues
  8. Able to review data within the Electronic Data Capture (EDC) and file management systems, perform and collate data downloads, reports, and prepare summaries of data extractions for review.
  9. Collaborate with CRAs, Data Management and vendors on data cleaning, tracking and data analysis quality.
  10. Assist in the production of presentations, etc., as needed for project, departmental, and/or business development presentations.
  11. Actively order and maintain ancillary clinical study supplies required for conduct of clinical trials.
  12. Assist with preparation, shipping, handling, distribution, and/or accountability of clinical trial supplies.
  13. Contribute to the development of clinical trial management best practice processes and Standard Operating Procedures (SOP).
  14. Maintain up-to-date knowledge of current regulations and guidelines to ensure compliance.
  15. Solve routine problems of limited scope and complexity following established policies and procedures.
  16. Work collaboratively with team to solve more complex issues.
  17. Other duties as assigned.


Requirements:

Skills

  1. Proficient in Microsoft Office applications (Word, Excel, and PowerPoint), Adobe and video/web conferencing. Knowledge of relational databases.
  2. Basic knowledge of clinical regulations and guidance including GCPs, and ICH guidelines.
  3. Excellent organizational skills, ability to manage multiple tasks and meticulous attention to detail.

Qualifications

Bachelor’s degree or equivalent and related work experience preferred. Excellent communication, teamwork, organizational, interpersonal, and problem-solving skills.

Working conditions

Office Environment, Laboratory Environment.

May be required to travel up to 15% of the time

Physical requirements

While performing the duties of this job, the employee is regularly required to sit for prolonged periods of time.

The employee may occasionally be required to pull, lift and/or move up to 20 pounds.

Direct reports

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job any time.