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Research Coordinator Jobs in Decatur, GA (NOW HIRING)

Caritas Medical Center

Be Seen First

Part time Research Coordinator

Stockbridge, GA · On-site

$25 - $30/hr

The Part Time Research Coordinator will primarily support clinical trials, playing a critical role in managing project logistics and maintaining high interaction with study participants. This role ...

DelRicht Research

Clinical Research Coordinator

Atlanta, GA

$23.75 - $31.75/hr

Clinical Research Coordinator's Main Objective: Overall, the Clinical Research Coordinator is responsible for providing quality, excellent patient care and a great experience for our patients in our ...

Hightop Health

Clinical Research Coordinator

Marietta, GA · On-site

$23 - $30.50/hr

The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and conduct of multiple clinical research trials at Hightop Health. This role provides both administrative and ...

Ora

Clinical Research Coordinator I

Hartford, CT

$24.50 - $32.50/hr

Clinical Research Coordinator I DEPARTMENT: Global Project Delivery *This role is a per-diem contract opportunity* Ora Values the Daily Practice of ... Prioritizing Kindness * Operational Excellence

Care Access

Clinical Research Coordinator II

Decatur, GA

$23.75 - $31.50/hr

How This Role Makes a Difference The Clinical Research Coordinator 's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely ...

CenExel

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

Under supervision, coordinates aspects of patient involvement for complex and/or multiple studies from study initiation until study completion. * Organizes research information for clinical trials.

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$18.2K

$68.3K

$95.3K

How much do research coordinator jobs pay per year?

As of May 30, 2026, the average yearly pay for research coordinator in Decatur, GA is $68,283.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,700.00 and $84,300.00 per year, depending on experience, location, and employer.

What Is a Research Coordinator?

A research coordinator supervises the daily activities of a study and monitors the activities of the subjects and researchers. As a research coordinator, your duties revolve around making sure that the study is conducted ethically and does not violate the research guidelines of the governing board or other agency. In short, you are responsible for making sure the study has as few flaws in its methodology as possible. You are also in charge of most administrative tasks. In this role, you can work on medical, technological, psychological, or other types of research projects, but you may work on clinical research most often.

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

To thrive as a Research Coordinator, you need strong organizational abilities, attention to detail, and a relevant bachelor's degree or higher in a scientific or health-related field. Familiarity with research compliance systems, data management tools, and Institutional Review Board (IRB) protocols is commonly required. Excellent communication, problem-solving, and multitasking skills help you manage studies and collaborate effectively with diverse teams. These skills ensure the smooth execution of research projects, regulatory compliance, and the reliability of study outcomes.

What are some common challenges Research Coordinators face when managing multiple studies simultaneously?

Research Coordinators often juggle several studies at once, which can present challenges such as balancing competing deadlines, ensuring compliance with regulatory requirements, and managing communication among diverse stakeholders. Staying organized with detailed documentation and proactive scheduling is essential to prevent protocol deviations. Effective collaboration with principal investigators, sponsors, and clinical staff also helps to navigate unexpected changes and maintain study integrity.

What are Research Coordinators?

Research Coordinators are professionals responsible for managing and overseeing research projects, often in academic, medical, or clinical settings. They help design studies, ensure compliance with regulations, recruit and communicate with participants, and manage data collection and documentation. Research Coordinators play a crucial role in keeping projects organized, on schedule, and in accordance with ethical and institutional guidelines. They often serve as a bridge between principal investigators, participants, and regulatory bodies.

What is the difference between Research Coordinator vs Research Assistant?

AspectResearch CoordinatorResearch Assistant
Required CredentialsBachelor's degree often required; some roles prefer or require a master'sTypically an undergraduate student or recent graduate; some roles may require a bachelor's degree
Work EnvironmentLeads study activities, manages protocols, interacts with stakeholdersSupports data collection, literature review, and administrative tasks
Employer & Industry UsageUsed in clinical, academic, and industry research settingsCommonly found in academic labs and research projects

The Research Coordinator generally has more responsibilities, including managing study protocols and liaising with stakeholders, while the Research Assistant provides support with data collection and administrative tasks. Both roles are essential in research projects but differ in scope and level of responsibility.

More about Research Coordinator jobs
What are the most commonly searched types of Research jobs in Decatur, GA? The most popular types of Research jobs in Decatur, GA are:
What are popular job titles related to Research Coordinator jobs in Decatur, GA? For Research Coordinator jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Research Coordinator jobs in Decatur, GA look for? The top searched job categories for Research Coordinator jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Research Coordinator jobs? Cities near Decatur, GA with the most Research Coordinator job openings:
Research Coordinator jobs near you
Infographic showing various Research Coordinator job openings in Decatur, GA as of May 2026, with employment types broken down into 85% Full Time, 6% Part Time, 6% Contract, and 3% Nights. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution, with an average salary of $68,283 per year, or $32.8 per hour.
Research Coordinator

Research Coordinator

Cardiovascular Associates of America

Tucker, GA • On-site

Contractor

This job post has expired today. Applications are no longer accepted.

Job description

Research Coordinator - Patient Screening & Enrollment
Location: On-site in Tucker, Georgia
Organization: Clinical Research Program (Cardiovascular Focus)
Great research starts with the right patients-and the clinical insight to identify them.
We're seeking a Research Coordinator - Patient Screening & Enrollment who brings both clinical judgment and operational precision to the front end of the clinical trial lifecycle. This role is ideal for someone who can interpret protocols, navigate medical records with confidence, and engage patients thoughtfully-even when that means initiating outreach.
If you're comfortable combining clinical knowledge, technology, and patient communication to drive enrollment success, this role was built for you.The Role
As the Research Coordinator - Patient Screening & Enrollment, you will lead patient identification and enrollment coordination for industry-sponsored clinical trials. You'll apply clinical skills to review protocols and medical records, use EMR systems to develop eligibility lists, and communicate directly with patients to support enrollment goals.
You'll work in close partnership with Principal Investigators (PIs), clinical teams, and research leadership to ensure studies enroll efficiently, ethically, and on schedule.What You'll Do
Clinical Screening & Eligibility Assessment
  • Review clinical trial protocols and apply inclusion/exclusion criteria accurately.
  • Conduct detailed medical record reviews to assess patient eligibility.
  • Collaborate with PIs and sub-investigators to confirm eligibility determinations.
  • Maintain precise documentation of screening decisions and eligibility status.
Technology & EMR-Based Identification
  • Use the electronic medical record (EMR) to identify potential study participants through chart review, reports, and registries.
  • Develop and maintain screening and recruitment lists aligned with protocol criteria.
  • Enter and track screening and enrollment activity in CTMS or other tracking systems.
Patient Outreach & Engagement
  • Conduct direct patient outreach, including phone calls and follow-up communications, to introduce research opportunities.
  • Confidently and professionally cold-call patients identified through EMR screening, using approved scripts and patient-centered communication.
  • Educate patients about study participation, next steps, and scheduling expectations.
Scheduling & Coordination
  • Schedule screening visits, study visits, and follow-up appointments in coordination with clinic workflows.
  • Ensure visit schedules align with protocol requirements and investigator availability.
Enrollment Tracking & PI Communication
  • Track enrollment progress against sponsor targets and timelines.
  • Provide PIs and site leadership with regular updates on screening pipelines and enrollment performance.
  • Identify and escalate barriers to enrollment and collaborate on solutions.
What We're Looking For
  • Clinical background or experience (e.g., RN, LPN, MA, CRC, or equivalent clinical research experience).
  • Demonstrated ability to read and interpret clinical trial protocols and medical records.
  • Strong proficiency with EMR systems and comfort navigating complex patient data.
  • Excellent communication skills, including comfort with outbound patient calls and cold outreach.
  • Strong organizational and time-management skills with attention to detail.
  • Experience with CTMS or research tracking tools (REALTIME-CTMS a plus).
  • A proactive, patient-focused professional who takes ownership of enrollment outcomes.
Ideal Experience
  • Prior experience in patient screening, recruitment, or enrollment for clinical trials.
  • Cardiovascular or specialty clinic experience.
  • Experience working in a fast-paced clinical environment with multiple protocols.
  • Comfort balancing clinical judgment with enrollment goals and sponsor expectations.
Why This Role Matters
Enrollment is the engine of clinical research. In this role, your clinical expertise, technical skills, and patient engagement directly determine whether studies succeed-and whether patients gain access to innovative therapies.

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