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

Clinical Research Coordinator

Atlanta, GA ยท On-site

$22 - $25/hr

Clinical Research Coordinator The Clinical Research Coordinator will support a post-market ... Handle study specimens in accordance with protocol and site procedures, without performing ...

Clinical Research Coordinator III

Atlanta, GA ยท On-site

$23.25 - $31/hr

The Clinical Research Coordinator III (CRC III) is responsible for leading the coordination and ... Study Management: * Ensure that study activities are conducted in accordance with GCP, IRB ...

CRC II (Onsite) - Marietta, GA

Marietta, GA ยท On-site

$23 - $30.50/hr

Clinical Conduct * Perform all study activities following Good Clinical Practices (GCP). * Manage ... Take the lead and/or overall coordination of clinic activities including, but not limited to:

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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 Aug 31, 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 are the key skills and qualifications needed to thrive as a clinical study coordinator?

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 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 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 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 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:

Infographic showing various Clinical Study Coordinator job openings in Decatur, GA as of August 2026, with employment types broken down into 3% As Needed, 69% Full Time, 20% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $65,943 per year, or $31.7 per hour.

Clinical Research Coordinator

Actalent

Atlanta, GA โ€ข On-site

$22 - $25/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Job Title: Clinical Research Coordinator

Job Description

The Clinical Research Coordinator will support a post-market respiratory testing study consisting of single study visits of approximately one hour. This contract role focuses on patient-facing coordination, data entry, and logistical support for the current research team, with the possibility of supporting additional studies depending on performance and future needs.

Responsibilities

  • Support patient enrollment into the post-market respiratory study, including pre-screening and eligibility confirmation.
  • Coordinate and schedule single study visits, ensuring participants understand the visit process and study requirements.
  • Enter study data accurately into REDCap and other electronic data capture (EDC) systems in a timely manner.
  • Use tablets and other study-related technology to collect and manage data during study visits.
  • Handle study specimens in accordance with protocol and site procedures, without performing laboratory testing.
  • Support administrative needs such as organizing and maintaining study supplies and materials.
  • Assist with documentation, including completion of study forms, logs, and regulatory records as required.
  • Collaborate with the broader study team to ensure protocol adherence and smooth day-to-day study coordination.
  • Adapt to support other study-related tasks or areas based on capability and evolving project needs.

Essential Skills

  • Clinical research experience, including at least one year in a clinical research setting; academic clinical research experience is acceptable.
  • Hands-on experience with electronic data capture (EDC) systems, preferably REDCap, or strong willingness and ability to learn new EDC platforms.
  • Demonstrated ability to review and follow clinical study protocols accurately.
  • Patient-facing experience, with comfort interacting directly with study participants in a clinical or research environment.
  • Strong attention to detail, particularly in data entry, documentation, and adherence to study procedures.
  • Comfort using tablets and learning new technology to support data collection and study operations.
  • Experience with pre-screening patients and managing patient enrollment processes for clinical studies.

Additional Skills & Qualifications

  • Experience with patient enrollment in clinical or research studies is considered a strong plus.
  • Ability to manage multiple study visits and tasks across different clinical sites.
  • Strong organizational and time-management skills to coordinate schedules and study logistics.
  • Effective communication skills to interact with patients and multidisciplinary clinical teams.
  • Flexibility to support additional studies or research activities as opportunities arise.

Work Environment

This role involves working across multiple clinical sites and requires independent travel between locations. The coordinator will need to transport themselves and arrange parking at various facilities, with no reimbursement provided for travel or parking. Schedules will be communicated in advance to allow for planning across different locations. The position is fully patient-facing and involves working with symptomatic respiratory patients, including individuals who may test positive for COVID. The environment includes active clinical settings such as hospitals and urgent care centers, where staff regularly use tablets, electronic data capture systems, and other study technologies during patient visits. Attire should be appropriate for clinical and hospital environments, reflecting professional standards and any site-specific guidelines.

Job Type & Location

This is a Contract position based out of Atlanta, GA.

Pay and Benefits

The pay range for this position is $22.00 - $25.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Atlanta,GA.

Application Deadline

This position is anticipated to close on Sep 7, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Industry

Business management consulting

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

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