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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 ...

Icon plc

Senior CRA

Atlanta, GA · On-site

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. * Conducting site visits to assess site performance ...

CenExel

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. Along with an exceptional work ...

CenExel

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. Along with an exceptional work ...

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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 Jul 18, 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, and why are they important?

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 are Clinical Trial Assistants?

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
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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
Clinical Trial Material Manager (2nd Shift)

Clinical Trial Material Manager (2nd Shift)

IQVIA

Marietta, GA • On-site

$77K - $161K/yr

Full-time

Medical, Life

Posted 3 days ago

New

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

55th of 210 rated it services

Job description

We are seeking Clinical Trial Material Manager (2nd Shift) to join IQVIA Laboratories at Marietta, GA.
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.
Job Summary:
The Clinical Trial Material Manager leads daily second-shift (2:00 PM to 11:00 PM) manufacturing operations in a regulated, high-volume production environment. This role ensures on-time delivery, quality compliance, staff performance, and continuous improvement while partnering across Project Services, Warehouse, Logistics, Quality, and IT.
What You'll Be Doing:
  • Lead, coach, and develop a team of direct reports in a dynamic production environment
  • Manage daily and long-range production schedules to meet customer demand and service-level production targets
  • Prioritize urgent, same-day, and future-dated work orders to ensure on-time delivery
  • Coordinate daily with Project Management, Warehouse, Logistics, Quality, and IT to resolve production issues and prevent delays
  • Utilize LIMS to support production files, platform reports, production metrics, dashboards, and compliance reporting
  • Perform root cause investigations for quality incidents, customer complaints, operations incidents, and in-process deviations
  • Lead and support Lean, Six Sigma, and process improvement initiatives to optimize production flow and reduce bottlenecks
What We Are Looking For:
  • Bachelor's degree, 10 years of experience in lieu of degree
  • Minimum 5 years of people management experience, managing 20 employees in a manufacturing environment
  • Minimum 5 years of experience managing manual assembly or production lines
  • Minimum 2 years of experience leading process improvement projects
  • Working knowledge of Microsoft Excel, Outlook, and PowerPoint
  • Working knowledge of ICH, GMP, and OSHA regulations
  • Six Sigma Yellow or Green Belt experience required; certification preferred
  • Other equivalent combination of education, training, and experience may be accepted in lieu of degree
The Knowledge, Skills and Abilities Needed for This Role:
  • Strong leadership, coaching, and staff development skills in a high-volume production environment
  • Ability to prioritize urgent and business-critical work while maintaining quality and compliance expectations
  • Effective cross-functional communication skills with the ability to escalate risks, constraints, and operational performance updates
  • Strong problem-solving skills with the ability to conduct investigations and drive root cause analysis
  • Ability to support overtime, weekends, and holidays based on critical business needs and accelerated trial timelines
What We Offer You:
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.
To learn more about our benefits, visit https://jobs.iqvia.com/benefits.
If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $77,700.00 - $161,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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Benefits

Hours and flexibility

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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