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

Georgia Institute of Technology

Research Assistant

Atlanta, GA · On-site

$18.50 - $25.50/hr

... clinical trial research by preparing human assurance protocols, informed consent documents, CRFs ... OR Associate's degree from an accredited college or university in chemistry, biology, biochemistry ...

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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 28, 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
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 Associate jobs in Decatur, GA? For Clinical Trial Associate jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Associate jobs in Decatur, GA look for? The top searched job categories for Clinical Trial Associate jobs in Decatur, GA are:
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 2% As Needed, 65% Full Time, and 33% Part Time. Highlights an 81% Physical, 4% Hybrid, and 15% Remote job distribution, with an average salary of $81,201 per year, or $39 per hour.
Associate Laboratory Project Services Manager (REMOTE)

Associate Laboratory Project Services Manager (REMOTE)

IQVIA

Marietta, GA • On-site, Remote

$64K - $133K/yr

Full-time

Medical, Life

Posted 5 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

46th of 206 rated it services

Job description

We are seeking Associate Laboratory Project Services Manager to join IQVIA Laboratories at Marietta, GA remotely.
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:
Under general direction, manage all laboratory aspects of clinical trial projects, serving as the main point of contact for customers throughout the study lifecycle. Ensure studies are delivered in alignment with standard operating procedures, policies, and best practices.
What You'll Be Doing:
  • Lead study setup activities including protocol and budget review, project planning, and risk and issue tracking
  • Coordinate with study setup teams to ensure quality database configuration and protocol-specific documentation
  • Monitor project timelines, deliverables, and documentation across the full study lifecycle including eTMF management
  • Manage study scope changes, budgets, and service quality while implementing improvements as needed
  • Act as the primary customer contact, building strong relationships and facilitating clear communication
  • Coordinate and resolve study-level issues, acting as an escalation point when required
  • Represent the company at investigator meetings, audits, and training sessions for sites and stakeholders
  • Support continuous improvement initiatives and assist in training less experienced team members
What We Are Looking For:
  • Bachelor's Degree in Life Sciences and/or related field preferred
  • 2+ years of clinical or research industry experience, including 1 year project management / project set up experience Pref Or Equivalent combination of education, training and experience
  • Working knowledge of central laboratory operations including logistics, specimen management, and data reporting
  • Proficiency in Microsoft Office and experience with centralized laboratory or project management systems
  • 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 interpersonal and customer relationship management skills
  • Ability to manage multiple priorities in a fast-paced environment while meeting deadlines
  • Effective written and verbal communication skills with strong attention to detail
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 $64,200.00 - $133,600.00. 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.

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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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