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

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

Coordination of Clinical Trials: * Oversee all aspects of assigned clinical studies, including start-up, recruitment, informed consent, data collection, and study close-out. Serve as the primary ...

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Clinical Trials Coordinator information

See Decatur, GA salary details

$27.3K

$65.9K

$113.3K

How much do clinical trials coordinator jobs pay per year?

As of Sep 3, 2026, the average yearly pay for clinical trials 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 is a clinical trials coordinator?

Clinical Trials Coordinators are professionals who manage and oversee the daily operations of clinical research studies. They ensure that studies are conducted according to regulatory guidelines, protocols, and ethical standards. Their responsibilities include recruiting and screening participants, collecting and managing study data, coordinating with investigators and sponsors, and ensuring compliance with protocols. They play a vital role in advancing medical research by facilitating the safe and effective testing of new treatments and therapies.

What are the key skills and qualifications needed to thrive as a clinical trials coordinator?

To thrive as a Clinical Trials Coordinator, you need strong organizational skills, knowledge of clinical research protocols, and a background in life sciences or a related field, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), regulatory compliance tools, and certifications such as Good Clinical Practice (GCP) are highly valued. Attention to detail, effective communication, and problem-solving abilities help ensure smooth collaboration among stakeholders and adherence to protocols. These skills are essential for ensuring regulatory compliance, data integrity, and the successful execution of clinical trials.

What are some common challenges faced by clinical trials coordinators, and how can they be effectively managed?

Clinical Trials Coordinators often encounter challenges such as strict regulatory compliance, managing multiple timelines, and coordinating communication among diverse stakeholders. Navigating complex protocols and ensuring accurate documentation are also critical aspects of the role. To effectively manage these challenges, coordinators benefit from strong organizational skills, attention to detail, and proactive communication with the research team, sponsors, and participants. Staying current with regulatory requirements and utilizing project management tools can also help streamline processes and reduce errors.

What are the most commonly searched types of Clinical Trials jobs in Decatur, GA?

The most popular types of Clinical Trials jobs in Decatur, GA are:

What job categories do people searching Clinical Trials Coordinator jobs in Decatur, GA look for?

The top searched job categories for Clinical Trials Coordinator jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Clinical Trials Coordinator jobs?

Cities near Decatur, GA with the most Clinical Trials Coordinator job openings:

Clinical Trials Coordinator jobs near you
Infographic showing various Clinical Trials Coordinator job openings in Decatur, GA as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 18% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $65,943 per year, or $31.7 per hour.

Clinical Research Coordinator III

Denali Health

Atlanta, GA • On-site

$70 - $100/hr

Other

Medical

Re-posted 3 days ago

Job description

About Denali Health:

Denali Health is a fast-growing clinical research organization dedicated to improving patient outcomes through innovative, high-quality clinical trials. We partner with leading physicians and sponsors to accelerate breakthrough treatments and foster greater access to research opportunities across diverse communities.

Position Summary:

The Clinical Research Coordinator III (CRC III) is responsible for leading the coordination and execution of complex clinical research studies, ensuring compliance with study protocols, regulatory requirements, and institutional guidelines. The ideal candidate is a proactive professional with strong organizational and leadership skills, capable of managing multiple studies and mentoring junior coordinators.

Key Responsibilities:
  • Coordination of Clinical Trials:
  • Oversee all aspects of assigned clinical studies, including start-up, recruitment, informed consent, data collection, and study close-out. Serve as the primary liaison between investigators, sponsors, CROs, and regulatory agencies.
  • Study Management:
  • Ensure that study activities are conducted in accordance with GCP, IRB guidelines, and sponsor requirements. Maintain accurate and up-to-date source documentation and regulatory binders.
  • Participant Coordination:
  • Schedule and coordinate participant visits, assessments, and follow-ups while maintaining excellent communication and care for study participants.
  • Regulatory and Compliance Oversight:
  • Prepare and submit IRB documents, safety reports, and study updates. Ensure audit readiness at all times.
  • Data Management:
  • Enter, review, and verify data in EDC systems and ensure timely query resolution.
  • Team Coordination & Leadership:
  • Mentor and support CRC I and II staff, ensuring consistent application of best practices and promoting a culture of quality and accountability.
  • Communication & Reporting:
  • Coordinate communication among multidisciplinary teams to ensure efficient trial operations and timely reporting of progress and outcomes.
Qualifications:
  • Bachelor’s degree in health sciences, nursing, or a related field (advanced degree preferred).
  • Minimum 3–5 years of experience in clinical research coordination.
  • Strong understanding of GCP, ICH, and FDA regulations.
  • Exceptional coordination, multitasking, and communication skills.
  • Experience with EDC systems and clinical trial management software preferred.
  • CCRC/CCRP certification a plus.
Why Join Denali Health:
  • Work with a mission-driven team advancing clinical research accessibility.
  • Competitive salary and comprehensive benefits package.
  • Professional growth and leadership opportunities.
  • Collaborative environment focused on innovation and patient care.
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