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

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global ... Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their ...

Amgen

Biostatistical Prograrmming Manager

Atlanta, GA · On-site

... and timely clinical trial deliverables. This role is part of the centrally managed Quality and ... OR Associate's degree and 8 years of statistical programming experience OR High school diploma ...

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

Clinical Trial Associate information

See Decatur, GA salary details

$16

$39

$68

How much do clinical trial associate jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for clinical trial associate in Decatur, GA is $39.04, according to ZipRecruiter salary data. Most workers in this role earn between $31.44 and $42.93 per hour, depending on experience, location, and employer.

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

AspectClinical Trial AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRABachelor's degree in health sciences or related field; similar certifications
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
ResponsibilitiesAssist in trial setup, data collection, regulatory complianceManage patient recruitment, conduct visits, data entry
Industry UsageCommon in pharmaceutical and biotech industriesCommon in hospitals and academic research settings

Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.

What Is a Clinical Trial Associate?

A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

What are some common challenges faced by Clinical Trial Associates when managing study documentation?

Clinical Trial Associates often encounter challenges related to maintaining accurate and up-to-date trial documentation, as protocols and regulatory requirements can change frequently. Ensuring all documents are correctly filed, version-controlled, and accessible for audits requires strong attention to detail and organizational skills. Additionally, coordinating with multiple stakeholders—such as clinical research coordinators, data managers, and regulatory teams—can add complexity to document management. Proactive communication and adopting robust documentation systems can help overcome these challenges.

What does a Clinical Trial Associate do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and management of clinical trials. They help ensure studies comply with regulatory requirements and assist in maintaining trial documentation, tracking study progress, and communicating with clinical sites. CTAs work closely with clinical research teams, sponsors, and vendors to keep trials running smoothly and efficiently. Their administrative and logistical support is essential for successful clinical research.

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

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These competencies are crucial for ensuring compliance, accurate data management, and smooth coordination of clinical trial activities.
More about Clinical Trial Associate jobs
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What cities near Decatur, GA are hiring for Clinical Trial Associate jobs? Cities near Decatur, GA with the most Clinical Trial Associate job openings:
Clinical Trial Associate jobs near you
Infographic showing various Clinical Trial Associate job openings in Decatur, GA as of June 2026, with employment types broken down into 1% Locum Tenens, 4% As Needed, 87% Full Time, 4% Part Time, 1% Temporary, and 3% Contract. Highlights an 70% Physical, 6% Hybrid, and 24% Remote job distribution, with an average salary of $81,201 per year, or $39 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.