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Protocol Coordinator Jobs in Georgia (NOW HIRING)

RN Research Coordinator

Marietta, GA ยท On-site

$62K - $78K/yr

The Research Coordinator has general responsibility for managing clinical trials for the Clinical ... Maintains current protocol with revisions, amendments and current IRB approved informed consent.

RN Research Coordinator

Marietta, GA ยท On-site

$65K - $81K/yr

The Research Coordinator has general responsibility for managing clinical trials for the Clinical ... Maintains current protocol with revisions, amendments and current IRB approved informed consent.

Resource Coordinator

Hinesville, GA ยท On-site

$35.22/hr

Under the general supervision of the Manager of Specialty Services, the Resource Coordinator is ... Collects data within established protocols and guidelines from various sources. Documents data ...

Resource Coordinator

Hinesville, GA ยท On-site

$35.22/hr

Under the general supervision of the Manager of Specialty Services, the Resource Coordinator is ... Collects data within established protocols and guidelines from various sources. Documents data ...

$11 - $14.50/hr

THE ROLE OF A COREPOWER YOGA STUDIO COORDINATOR As a Studio Coordinator (SC), you live your power ... Support communication around Smart Health Protocol to students upon entry and throughout their ...

... protocols, and hospital policies. * Participate in quality improvement initiatives, monitoring ... Experience in patient care coordination, quality improvement, and leadership preferred.

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Protocol Coordinator information

See Georgia salary details

$22.8K

$48.9K

$85.7K

How much do protocol coordinator jobs pay per year?

As of Aug 31, 2026, the average yearly pay for protocol coordinator in Georgia is $48,863.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,200.00 and $58,700.00 per year, depending on experience, location, and employer.

What is a protocol coordinator?

Protocol coordinators are professionals responsible for managing and overseeing the implementation of clinical trial protocols or research studies. They ensure that all activities are conducted in compliance with regulatory requirements, ethical standards, and the specific guidelines of the study protocol. Their duties often include organizing study logistics, coordinating communications between investigators and sponsors, maintaining accurate documentation, and ensuring participant safety. Protocol coordinators play a crucial role in ensuring the smooth and efficient operation of clinical research projects.

What are the key skills and qualifications needed to thrive as a protocol coordinator, and why are they important?

To thrive as a Protocol Coordinator, you need strong organizational skills, attention to detail, and a background in clinical research or project management, often supported by a relevant bachelor's degree. Familiarity with regulatory compliance systems, clinical trial management software (CTMS), and protocols such as Good Clinical Practice (GCP) is typically required. Excellent communication, problem-solving, and multitasking abilities help you effectively coordinate between stakeholders and manage complex timelines. These skills ensure the smooth execution of protocols, regulatory compliance, and the successful progression of clinical studies or organizational processes.

What are some common challenges protocol coordinators face when managing complex meetings or events?

Protocol Coordinators often encounter challenges such as balancing the needs and expectations of diverse stakeholders, ensuring strict adherence to diplomatic protocols, and managing last-minute changes in schedules or guest lists. Successfully navigating cultural sensitivities and maintaining effective communication with both internal teams and external partners are key to overcoming these obstacles. Flexibility, attention to detail, and strong organizational skills are essential for addressing unexpected issues while maintaining a professional environment.

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

AspectProtocol CoordinatorClinical Research Associate
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCRP are a plusUsually a bachelor's degree in life sciences or health sciences; certifications like CCRP or CRA are common
Work EnvironmentOffice-based, coordinating clinical trial protocols, communicating with sites and teamsMonitoring clinical sites, ensuring compliance, and data accuracy during trials
Employer & Industry UsagePharmaceutical companies, research institutions, CROsPharmaceutical companies, CROs, research organizations

While both roles support clinical trials, Protocol Coordinators focus on managing trial protocols and communication, whereas Clinical Research Associates primarily monitor trial sites and ensure compliance. Both roles require similar educational backgrounds and certifications, often working within the same industry environments.

How long does it take to become a protocol coordinator?

Becoming a protocol coordinator typically requires a bachelor's degree in a related field such as healthcare, life sciences, or research, which takes about four years. Gaining relevant experience in clinical research or project management can take an additional 1-3 years, depending on the individual's background and the complexity of the role.

What are the most commonly searched types of Protocol jobs in Georgia?

The most popular types of Protocol jobs in Georgia are:

What are popular job titles related to Protocol Coordinator jobs in Georgia?

For Protocol Coordinator jobs in Georgia, the most frequently searched job titles are:

What cities in Georgia are hiring for Protocol Coordinator jobs?

Cities in Georgia with the most Protocol Coordinator job openings:

Infographic showing various Protocol Coordinator job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 13% Part Time, 1% Temporary, 6% Contract, and 3% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $48,863 per year, or $23.5 per hour.

Clinical Trials RN Coordinator - Research & Protocol Lead

Marietta, GA โ€ข On-site

Full-time

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


Job description

Wellstar Health System, Inc. in Marietta, Georgia is seeking a Research Coordinator to manage clinical trials, including patient eligibility and ongoing care. The role requires a strong RN background with at least 5 years of experience, alongside expertise in research and critical care. Responsibilities include coordinating patient therapy initiation, maintaining records, communicating with medical staff, and ensuring compliance with regulatory guidelines. Ideal candidates possess excellent communication and organizational skills.