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Clinical Data Associate Jobs in Augusta, GA (NOW HIRING)

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Clinical Data Associate information

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How much do clinical data associate jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical data associate in Augusta, GA is $36.61, according to ZipRecruiter salary data. Most workers in this role earn between $27.55 and $36.59 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Augusta, GA?

The most popular types of Clinical Data jobs in Augusta, GA are:

What are popular job titles related to Clinical Data Associate jobs in Augusta, GA?

For Clinical Data Associate jobs in Augusta, GA, the most frequently searched job titles are:

What job categories do people searching Clinical Data Associate jobs in Augusta, GA look for?

The top searched job categories for Clinical Data Associate jobs in Augusta, GA are:

What cities near Augusta, GA are hiring for Clinical Data Associate jobs?

Cities near Augusta, GA with the most Clinical Data Associate job openings:

Infographic showing various Clinical Data Associate job openings in Augusta, GA as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $76,159 per year, or $36.6 per hour.

Full-time

Re-posted 5 days ago


Job description

Position Summary

The Quality Manager supports the mission and vision of Medical Associates Plus by coordinating, implementing, and monitoring clinical quality improvement activities across provider and practice sites. This position works closely with the Chief Medical Officer, Quality leadership, and clinical operations teams to support quality initiatives, regulatory compliance, patient safety, and continuous quality improvement (CQI) efforts.

The Quality Manager assists with the organization’s Quality Improvement, Risk Management, and Infection Control programs by monitoring performance measures, analyzing clinical data, supporting compliance activities, and helping develop strategies to improve patient outcomes. This role collaborates with clinical and operational teams to promote high-quality patient care and ensure compliance with Health Resources and Services Administration (HRSA) Health Center Program requirements, FTCA, PCMH, and other applicable healthcare regulations.


Responsibilities and Duties

Duties include but are not limited to:

  • Collaborate with the Chief Medical Officer and leadership team to support achievement of Quality Performance Measures, FTCA, PCMH, and organizational quality goals.
  • Support the development, implementation, and monitoring of the organization’s Continuous Quality Improvement (CQI) program, including quality improvement initiatives, utilization management, and risk management activities.
  • Assist with identifying opportunities for improvement through data analysis, audits, performance measures, and staff feedback.
  • Educate staff and providers regarding quality improvement processes, compliance requirements, and organizational standards.
  • Coordinate quality improvement projects across clinical and operational departments.
  • Assist with preparing quality reports, presentations, and updates for leadership, committees, and regulatory requirements.
  • Support scheduling, coordination, documentation, and reporting of peer reviews and quality-related activities.
  • Assist with clinical safety and risk management initiatives, including review and maintenance of safety policies and procedures.
  • Collaborate with Clinical and Operations Managers to address patient complaints, quality concerns, and opportunities for improvement.
  • Serve as a resource and liaison between providers, clinical teams, and internal departments regarding quality initiatives.
  • Participate in quality committees, including CQI and Risk Management meetings.
  • Assist with monitoring compliance with clinical regulatory standards, including HRSA Health Center Program requirements, FTCA, PCMH, CLIA, OSHA, and other applicable regulations.
  • Support the Infection Control program through policy review, staff education, audits, and compliance monitoring.
  • Assist with monitoring clinical supplies, vaccines, and safety requirements across sites.
  • Support the QI Committee by tracking action items, monitoring corrective actions, and following up on improvement plans.
  • Maintain and update clinical policies, procedures, and quality-related documentation.
  • Monitor adherence to clinical protocols and evidence-based practices.
  • Collect, analyze, and report clinical performance data for UDS reporting, HRSA requirements, and organizational quality initiatives.
  • Assist with completion of clinical components of the UDS report, including data validation, reporting, and participation in related trainings.
  • Monitor documentation and compliance related to sample medications, EHR entries, and required tracking logs.
  • Assist with FTCA application preparation and required documentation submission.
  • Support maintenance and optimization of eClinicalWorks templates, alerts, and workflows to promote compliance with ACO, PCMH, SAC, NAP, Medicare, and other quality initiatives.
  • Assist with maintaining PCMH recognition requirements across organizational sites.
  • Support care coordination efforts, including care transitions and post-discharge follow-up processes.
  • Participate in quality-related orientation and training for new employees.
  • Serve as a support resource for emergency preparedness and disaster response activities.
  • Maintain strict confidentiality regarding patients, employees, and organizational information.
  • Uphold Medical Associates Plus’ Mission, Values, and Standards of Conduct.
  • Perform other duties as assigned.

Qualifications

Knowledge, Skills, and Abilities

  • Strong interpersonal and communication skills.
  • Ability to build effective working relationships with providers, clinical staff, leadership, and external partners.
  • Strong organizational skills with the ability to manage multiple priorities and deadlines.
  • Knowledge of healthcare quality improvement principles and performance improvement methodologies.
  • Ability to collect, analyze, interpret, and present healthcare data.
  • Understanding of federal and state healthcare compliance requirements.
  • Knowledge of primary care operations, patient safety, and evidence-based practices.
  • Familiarity with FQHC operations, HRSA requirements, FTCA, PCMH, UDS reporting, and quality measures preferred.
  • Knowledge of infection prevention and employee safety practices.
  • Strong problem-solving skills with attention to detail and accuracy.
  • Ability to work independently while collaborating effectively with cross-functional teams.
  • Proficiency with electronic health record systems, especially eClinicalWorks, preferred.

Education and Licensure Requirements

  • Bachelor’s degree from an accredited institution required.
  • Master’s degree in Healthcare Administration, Nursing, Public Health, Quality Management, or a related field preferred.
  • Clinical background or healthcare quality certification preferred.

Experience

  • Experience working in healthcare quality improvement, compliance, clinical operations, or related healthcare setting required.
  • Experience in a Federally Qualified Health Center (FQHC) or community health setting preferred.
  • Experience with quality reporting, audits, performance measures, and regulatory requirements preferred.
  • Experience working with electronic health records, particularly eClinicalWorks, preferred.
  • Ability to manage multiple projects, prioritize tasks, and meet deadlines in a fast-paced healthcare environment.

Physical Demands

Must be able to perform all duties with or without reasonable accommodation.

  • Ability to sit or stand for extended periods.
  • Occasional lifting of up to 30 pounds.
  • Manual dexterity sufficient to operate a keyboard and office equipment.
  • Sufficient vision and hearing (with or without accommodations) to perform job duties.
  • Ability to move throughout clinical and administrative areas as needed.
  • Ability to work collaboratively with diverse teams and respond effectively to interruptions.

Working Conditions

  • Combination of office and clinical healthcare environments.
  • Regular interaction with patients, employees, providers, leadership, vendors, and community partners.
  • May require occasional extended hours, evenings, or weekends based on organizational needs.
  • Requires professionalism, confidentiality, discretion, and sound judgment.

Disclaimer

The above is intended to describe the general job functions, responsibilities, and requirements for this position. It is not intended to be an exhaustive list of all duties, responsibilities, or qualifications required. Additional responsibilities may be assigned based on organizational needs.

Medical Associates Plus is an Equal Opportunity Employer and does not discriminate against any employee or applicant because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, veteran status, disability, or any other federally, state, or locally protected classification.