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Clinical Research Coordinator Rheumatology Jobs in Decatur, GA

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Clinical Research Coordinator

Johns Creek, GA · On-site

$22.50 - $30/hr

Clinical Research Coordinator ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

ICON

Clinical Research Coordinator

Johns Creek, GA · On-site

$22.50 - $30/hr

Clinical Research Coordinator ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

IQVIA

Clinical Research Coordinator

Marietta, GA

$35 - $42/hr

Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours/week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...

Georgia Retina

Clinical Research Coordinator

Marietta, GA · On-site

$23 - $30.50/hr

Responsibilities A CRA is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols. • Recruit and screen subjects to participate ...

Georgia Retina

Clinical Research Coordinator

Marietta, GA

$23 - $30.50/hr

Responsibilities A CRA is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols. Recruit and screen subjects to participate in ...

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

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 ...

Clayton Eye Center

Clinical Research Coordinator

Morrow, GA · On-site

$23 - $30.75/hr

Responsibilities A Research Coordinator I will be expected to meet the following performance ... clinical research • Analytical mindset • Attention to detail • Exceptional interpersonal ...

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 ...

Alcanza

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. Essential Job Duties: In collaboration with ...

Care Access

Clinical Research Coordinator II

Decatur, GA · On-site

$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 ...

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Clinical Research Coordinator Rheumatology information

See Decatur, GA salary details

$15

$28

$41

How much do clinical research coordinator rheumatology jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical research coordinator rheumatology 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 are the key skills and qualifications needed to thrive as a clinical research coordinator in rheumatology?

To thrive as a Clinical Research Coordinator in Rheumatology, you need a background in life sciences or healthcare, experience in clinical trial management, and knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and certifications like ACRP or SOCRA is highly valued. Strong organizational skills, attention to detail, and effective communication are crucial for managing studies and collaborating with diverse teams. These skills ensure the integrity of research, patient safety, and compliance with complex regulatory requirements in rheumatology trials.

What does a clinical research coordinator in rheumatology do?

A Clinical Research Coordinator (CRC) in Rheumatology is responsible for managing clinical trials and research studies focused on rheumatic diseases, such as arthritis and lupus. Their duties include recruiting and enrolling patients, ensuring studies comply with ethical and regulatory requirements, collecting and managing data, and coordinating with physicians and research staff. The CRC also helps with patient education, scheduling study visits, and maintaining accurate records to ensure the integrity of research data. They play a key role in advancing rheumatology treatment options through high-quality clinical research.

What are some common challenges faced by clinical research coordinators in rheumatology studies?

Clinical Research Coordinators in Rheumatology often encounter challenges such as managing complex protocols for multiple ongoing studies, ensuring patient retention over long study periods, and handling diverse data collection requirements. Coordinators must also navigate frequent communication with multidisciplinary teams, including physicians, nurses, and data managers, while keeping up with regulatory documentation. Developing strong organizational skills and building rapport with patients can help address these challenges and contribute to the success of clinical trials.

What is the difference between Clinical Research Coordinator Rheumatology vs Clinical Research Coordinator Oncology?

AspectClinical Research Coordinator RheumatologyClinical Research Coordinator Oncology
Required CredentialsBS or BA, clinical research certification preferredBS or BA, clinical research certification preferred
Work EnvironmentRheumatology clinics, hospitals, research centersOncology clinics, hospitals, research centers
Employer & Industry UsageMedical research institutions, hospitals, pharmaceutical companiesHospitals, cancer centers, pharmaceutical companies
Common Search & ComparisonYesYes

The Clinical Research Coordinator Rheumatology and Clinical Research Coordinator Oncology roles share similar credentials, work environments, and employer types. The main difference lies in the medical specialty focus: rheumatology involves autoimmune and musculoskeletal diseases, while oncology centers on cancer research. Both roles require coordination of clinical trials, patient interaction, and adherence to regulatory standards, but their specific disease focus distinguishes them.

What job categories do people searching Clinical Research Coordinator Rheumatology jobs in Decatur, GA look for? The top searched job categories for Clinical Research Coordinator Rheumatology jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Research Coordinator Rheumatology jobs? Cities near Decatur, GA with the most Clinical Research Coordinator Rheumatology job openings:
Clinical Research Coordinator Rheumatology jobs near you

Clinical Research Coordinator

Alcanza Clinical Research

Decatur, GA • On-site

$23.75 - $31.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 2 days ago

Job description

Clinical Research Coordinator
Department: Operations
Employment Type: Full Time
Location: Accel Research Sites - Decatur, GA
Reporting To: Benoit Tete
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.
Key Responsibilities
Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
  • Screening of patients for study enrollment;
  • Patient consents;
  • Patient follow-up visits;
  • Documenting in source clinic charts;
  • Entering data in EDC and answers queries;
  • Obtaining vital signs and ECGs;
  • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
  • Requesting and tracking medical record requests;
  • Updating and maintaining logs, chart filings;
  • Maintaining & ordering study specific supplies;]
  • Scheduling subjects for study visits and conducts appointment reminders;
  • Building/updating source as needed;
  • Conducting monitoring visits and resolves issues as needed in a timely manner;
  • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
  • Filing SAE/Deviation reports to Sponsor and IRB as needed;
  • Documenting and reporting adverse events;
  • Reporting non-compliance to appropriate staff in timely manner;
  • Maintaining positive and effective communication with clients and team members;
  • Always practicing ALCOAC principles with all documentation;
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • Maintaining confidentiality of patients, customers and company information, and;
  • Performing all other duties as requested or assigned.
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
  • May set up, train and maintain all technology needed for studies.

Skills, Knowledge and Expertise
Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. Bi-lingual (English / Spanish) proficiency is a plus.
Required Skills:
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

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