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Clinical Research Coordinator Jobs in Decatur, GA

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$15

$28

$41

How much do clinical research coordinator jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical research coordinator in Decatur, GA is $28.01, according to ZipRecruiter salary data. Most workers in this role earn between $22.79 and $30.29 per hour, depending on experience, location, and employer.

What is a clinical research coordinator?

A Clinical Research Coordinator (CRC) is a professional who manages and oversees clinical trials and research studies involving human participants. They are responsible for ensuring that studies are conducted according to protocol, regulatory requirements, and ethical standards. CRCs handle tasks such as recruiting participants, collecting and managing data, coordinating with research teams, and maintaining documentation. Their work is essential in advancing medical knowledge and ensuring the safety and rights of study participants.

What is a clinical research coordinator?

As a clinical research coordinator, your responsibilities and duties include overseeing research volunteers during medical trials for new drugs and medical devices. You train the volunteers and educate them about the trial and the rules they must follow. You also record data that they report and ensure they are doing the research ethically. Your job is to work with trial subjects, oversee the administration of medication or device usage, and conduct data collection accurately so that the results are as sound as possible. You must also report any unethical practices or concerns regarding trial volunteers to the doctors doing this research.

What are some common challenges faced by clinical research coordinators when managing multiple studies simultaneously?

Clinical Research Coordinators often manage several studies at once, which can present challenges in balancing timelines, documentation, and communication with various stakeholders. Keeping track of regulatory requirements, participant schedules, and data integrity for each study requires strong organizational skills and adaptability. Coordinators frequently collaborate with investigators, sponsors, and clinical staff to ensure protocol adherence and resolve issues quickly, making effective multitasking and prioritization essential to success in this role.

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

To thrive as a Clinical Research Coordinator, you need strong organizational abilities, attention to detail, and knowledge of clinical trial processes, often supported by a degree in life sciences or healthcare. Familiarity with regulatory compliance systems (such as GCP), electronic data capture (EDC) tools, and certifications like ACRP or SOCRA are typically required. Excellent communication, problem-solving, and teamwork skills enable effective coordination among investigators, sponsors, and patients. These competencies are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting the overall success of clinical research studies.

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

AspectClinical Research CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonOften requires a bachelor's or master's degree; certifications like CCRP or RAC are advantageous
Work EnvironmentWorks primarily at research sites, hospitals, or clinicsWorks mainly at sponsor offices, CROs, or monitoring sites
Employer & IndustryResearch institutions, hospitals, clinicsPharmaceutical companies, CROs, biotech firms
Job FocusManages daily study activities, patient recruitment, data collectionMonitors study progress, ensures compliance, verifies data accuracy

While both roles support clinical trials, Clinical Research Coordinators handle on-site study management and patient interactions, whereas Clinical Research Associates focus on monitoring and compliance from a remote or office setting. Understanding these differences helps in choosing the right career path or job search focus.

What qualifications do you need to be a clinical research coordinator?

A clinical research coordinator typically needs a bachelor's degree in health sciences, biology, or a related field. Relevant experience in clinical settings, strong organizational skills, and knowledge of Good Clinical Practice (GCP) guidelines are also important; some positions may require certification such as the Certified Clinical Research Coordinator (CCRC).
More about Clinical Research Coordinator jobs

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

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

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

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

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

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

Clinical Research Coordinator jobs near you
Infographic showing various Clinical Research Coordinator job openings in Decatur, GA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $58,254 per year, or $28 per hour.

Clinical Research Coordinator III - Pediatrics, Nephrology

Jobtailor

Atlanta, GA • On-site

$100 - $150/hr

Other

Posted 3 days ago

New

Job description

  • Independently manage significant and key aspects of a large clinical trial or all aspects of one or more small trials or research projects
  • Train and provide guidance to less experienced staff
  • Oversee data management for research projects
  • Interface with research participants and resolve issues related to study protocols
  • Authorize purchases for supplies and equipment maintenance
  • Determine effective strategies for promoting, recruiting, and retaining research participants in long-term clinical trials
  • Periodically audit operations, including laboratory procedures, to ensure compliance with applicable regulations
  • Provide leadership in identifying and implementing corrective actions and processes
  • Monitor IRB submissions and respond to requests and questions
  • Interface with study sponsors and monitors
  • Report serious adverse events (SAEs) and resolve study queries
  • Provide leadership in determining, recommending, and implementing policy and process improvements
  • Assist in developing grant proposals and protocols
  • Perform phlebotomy, specimen collection, or diagnostics when appropriately credentialed and trained
  • May perform some supervisory duties
  • Perform related approved responsibilities as required
Requirements
  • High School Diploma or GED and seven years of clinical research experience; or
  • Two years of college in a scientific, health related or business administration program and five years of clinical research experience; or
  • Licensed as a Practical Nurse (LPN) and four years of clinical research experience; or
  • Bachelor's degree in a scientific, health related or business administration program and three years of clinical research experience; or
  • Master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience
  • Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred
  • Position involves clinical patient contact
  • All clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher
Core Competencies

Demonstrates expertise in managing clinical trials, including participant recruitment, data management, and compliance with regulations. Proficient in providing leadership and training to staff while ensuring adherence to study protocols and operational audits.

Highest-signal resume keywords
  • Clinical Trial Management
  • Data Management
  • Participant Recruitment
  • Regulatory Compliance
  • Leadership in Clinical Research
Hard Skills
  • Phlebotomy
  • Specimen Collection
  • Diagnostics
  • Grant Proposal Development
  • Protocol Development
Soft Skills
  • Training and Guidance
  • Problem Resolution
  • Communication with Participants
Certifications & Qualifications
  • Certified Research Administrator (CRA)
  • Clinical Research Coordinator (CRC)
Industry Keywords
  • Clinical Research
  • Compliance Regulations
  • Adverse Event Reporting
  • Laboratory Procedures
  • Clinical Patient Contact
Tools & Technologies
  • IRB Submission Monitoring
  • Clinical Research Software
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