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Clinical Study Coordinator Jobs in Decatur, GA (NOW HIRING)

Care Access

Clinical Research Coordinator II

Decatur, GA · On-site

$23.75 - $31.50/hr

Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with ... A minimum of 3 years prior Clinical Research Coordinator experience required * Prefer 1 year of ...

Care Access

Clinical Research Coordinator II

Decatur, GA

$23.75 - $31.50/hr

Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with ... A minimum of 3 years prior Clinical Research Coordinator experience required  * Prefer 1 year of ...

Alcanza

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

We have established a strong presence across Phase I-IV studies and several therapeutic areas ... The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in ...

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Clinical Study Coordinator information

See Decatur, GA salary details

$27.3K

$65.9K

$113.3K

How much do clinical study coordinator jobs pay per year?

As of Jun 11, 2026, the average yearly pay for clinical study coordinator in Decatur, GA is $65,943.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,200.00 and $76,600.00 per year, depending on experience, location, and employer.

What does a Clinical Study Coordinator do?

A Clinical Study Coordinator is responsible for managing and overseeing clinical trials and research studies to ensure they run smoothly and comply with regulatory requirements. Their duties include recruiting and screening participants, collecting and managing data, coordinating with research staff and physicians, and ensuring that all study protocols are followed accurately. They also handle scheduling, documentation, and may assist with regulatory submissions to ethics boards. In essence, they serve as the main point of contact for the study and help ensure its successful completion.

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

AspectClinical Study CoordinatorClinical Research Associate
Required CredentialsTypically a bachelor's degree in health sciences or related field; certifications like CCRP are a plusOften a bachelor's degree in life sciences; certifications like CCRP or RAC are common
Work EnvironmentConducts site visits, manages study activities at clinical sitesMonitors multiple sites remotely or on-site, ensuring protocol compliance
Employer & Industry UsageHospitals, clinics, research sitesPharmaceutical companies, CROs, biotech firms

While both roles support clinical research, Clinical Study Coordinators focus on managing day-to-day site activities, whereas Clinical Research Associates primarily monitor and oversee multiple sites to ensure regulatory compliance and data integrity.

What are some common challenges Clinical Study Coordinators face when managing multiple studies at once?

Clinical Study Coordinators often juggle several studies simultaneously, which requires strong organizational and time-management skills. Challenges include prioritizing tasks, ensuring regulatory compliance across different protocols, and keeping accurate documentation for each study. Effective communication with investigators, sponsors, and participants is essential to prevent misunderstandings and maintain study timelines. Utilizing project management tools and maintaining up-to-date records can help coordinators stay on track and reduce stress.

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

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, IRB submission processes, and Good Clinical Practice (GCP) certification is highly valued. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating study teams and liaising with stakeholders. These abilities ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, safeguarding both data integrity and participant safety.
What are the most commonly searched types of Clinical Study jobs in Decatur, GA? The most popular types of Clinical Study jobs in Decatur, GA are:
What are popular job titles related to Clinical Study Coordinator jobs in Decatur, GA? For Clinical Study Coordinator jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Clinical Study Coordinator jobs in Decatur, GA look for? The top searched job categories for Clinical Study Coordinator jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Study Coordinator jobs? Cities near Decatur, GA with the most Clinical Study Coordinator job openings:
Clinical Study Coordinator jobs near you
Clinical Research Coordinator, On-site, Lilburn, GA

Clinical Research Coordinator, On-site, Lilburn, GA

IQVIA

Lilburn, GA

$36K - $91K/yr

Full-time

Posted 26 days ago

IQVIA rating

8.2

Company rating: 8.2 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

46th of 204 rated it services

Job description

This is a fully on-site position in Lilburn, GA.

Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.

Why Avacare?
At Avacare, CRCs wear more hats than in traditional research settings. You'll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities - from patient recruitment and informed consent to regulatory documentation and site audits. This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond.

What You'll Gain:

Broadened Skill Set: Manage 2-6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
Professional Growth: Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training.
Collaborative Culture: Be part of a supportive team that values initiative, adaptability, and continuous learning.
Global Impact: Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.

Qualifications:
Clinical Skills: Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
Site Operations Knowledge: Solid understanding of site operations and the drug development process.


Experience:
CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.
CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.
Communication & Documentation: Strong written and verbal communication skills, with attention to detail and time management.
Technical Proficiency: Comfortable using CTMS, eCRFs, and Microsoft Office tools.

Whether you're early in your CRC journey or ready to take the next step, Avacare offers a unique environment where your contributions matter and your career can flourish.

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 $36,600.00 - $91,300.00. 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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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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