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Clinical Research Regulatory Assistant Jobs in Decatur, GA

Maintain regulatory compliance with FDA, ICH-GCP, and institutional guidelines * Coordinate with ... CROs * Assist with patient recruitment and retention activities * Maintain study supplies ...

Maintain regulatory compliance with FDA, ICH-GCP, and institutional guidelines * Coordinate with ... CROs * Assist with patient recruitment and retention activities * Maintain study supplies ...

Clinical Research Coordinator

Marietta, GA · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position Summary We are now hiring for a Clinical Research Assistant that will support a high ... regulatory and ethical standards Maintain relationships with site staff, study subjects, and ...

Clinical Research Coordinator

Atlanta, GA · On-site

$22 - $25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... * Assist with documentation, including completion of study forms, logs, and regulatory records as ... Clinical research experience, including at least one year in a clinical research setting; academic ...

New

Clinical Research Coordinator

Atlanta, GA · On-site

$22 - $25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... * Assist with documentation, including completion of study forms, logs, and regulatory records as ... Clinical research experience, including at least one year in a clinical research setting; academic ...

New

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

  • Medical

Regulatory and Compliance Oversight: * Prepare and submit IRB documents, safety reports, and study updates. Ensure audit readiness at all times. * Data Management: * Enter, review, and verify data in ...

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Regulations and SOPs. Essential Job Duties: In collaboration with other members of the clinical ... May assist with study recruitment, patient enrollment, and tracking as needed; * Maintaining ...

Research Assistant

Atlanta, GA · On-site

$18.50 - $25.50/hr

Support Clinical Research Visits: * Assist with participant visits and study-related procedures ... regulatory guidelines. Perform Clinical Procedures: * Perform venipuncture and blood collection ...

Clinical Research Nurse

Decatur, GA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Regulations and SOPs. Essential Job Duties: In collaboration with other members of the clinical ... May assist with study recruitment, patient enrollment, and tracking as needed; * Maintaining ...

Showing results 21-40

Clinical Research Regulatory Assistant information

See Decatur, GA salary details

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How much do clinical research regulatory assistant jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for clinical research regulatory assistant in Decatur, GA is $22.17, according to ZipRecruiter salary data. Most workers in this role earn between $16.88 and $25.34 per hour, depending on experience, location, and employer.

What does a clinical research regulatory assistant do?

A Clinical Research Regulatory Assistant supports clinical research teams by ensuring that all research activities comply with regulatory requirements and institutional policies. Their duties typically include preparing and submitting documents to Institutional Review Boards (IRBs), maintaining regulatory files, tracking study approvals, and assisting with audits. They play a key role in ensuring that clinical trials are conducted ethically and according to legal standards, helping protect study participants and maintain the integrity of research data.

What are the key skills and qualifications needed to thrive as a clinical research regulatory assistant?

To thrive as a Clinical Research Regulatory Assistant, you need a strong understanding of clinical research processes, regulatory compliance, and documentation, often supported by a bachelor's degree in life sciences or a related field. Familiarity with regulatory systems such as IRB portals, electronic document management systems, and GCP (Good Clinical Practice) guidelines is typically required. Attention to detail, strong organizational skills, and effective communication help you excel in managing complex documentation and coordinating with multiple stakeholders. These skills are crucial for ensuring regulatory requirements are met, which protects study integrity and supports the success of clinical trials.

What are the main challenges a clinical research regulatory assistant may face when managing multiple study protocols?

A Clinical Research Regulatory Assistant often juggles several study protocols at once, each with its own set of regulatory requirements and deadlines. One common challenge is ensuring timely and accurate submission of documents to regulatory bodies while keeping up with frequent updates or amendments from study sponsors. Effective organization, attention to detail, and strong communication with study coordinators and principal investigators are crucial to prevent delays and maintain compliance. Prioritizing tasks and leveraging tracking tools can help manage these responsibilities efficiently.

What is the difference between Clinical Research Regulatory Assistant vs Clinical Research Coordinator?

AspectClinical Research Regulatory AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health, life sciences, or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications like CCRP or RAC are common
Work EnvironmentSupports regulatory documentation, compliance, and submissions; often works in offices or labsManages study participants, coordinates activities, and oversees daily trial operations
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for regulatory tasksEmployed by hospitals, research centers, and clinics to oversee clinical trial processes

While both roles support clinical research, the Clinical Research Regulatory Assistant focuses on regulatory compliance and documentation, whereas the Clinical Research Coordinator manages study operations and participant interactions. Understanding these differences helps in choosing the right career path or job search focus.

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

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

What are popular job titles related to Clinical Research Regulatory Assistant jobs in Decatur, GA?

For Clinical Research Regulatory Assistant jobs in Decatur, GA, the most frequently searched job titles are:

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

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

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

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

Clinical Research Coordinator I (ETS) | Temporary

Emory University

Atlanta, GA • On-site

$23.50 - $31.50/hr

Full-time, Temporary

Re-posted 12 days ago


Emory Healthcare rating

7.7

Company rating: 7.7 out of 10

Based on 217 frontline employees who took The Breakroom Quiz

159th of 889 rated healthcare providers


Job description

Discover Your Career at Emory University

Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community.

Description

The Clinical Research Coordinator provides essential support across the full spectrum of research activities, including clinical and preclinical translational studies. This role is responsible for assisting with regulatory submissions (IRB and IACUC), coordinating clinical study operations, and contributing to the preparation of scientific manuscripts and extramural grant applications. The ideal candidate is detail-oriented, scientifically fluent, and capable of managing multiple concurrent projects in a fast-paced research environment. 

KEY RESPONSIBILITIES:

  • Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
  • Assists with patient recruitment.
  • Attends study meetings.
  • Orders and maintains equipment and supplies.
  • Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
  • Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
  • Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
  • Assists with quality assurance and tracks regulatory submissions.
  • Performs related approved responsibilities as required.

MINIMUM QUALIFICATIONS:

  • High School Diploma or GED and three years of administrative support experience.
  • Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience.
  • Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience.
  • Or a Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.

PREFERRED QUALIFICATIONS: 

  • Bachelor's degree in a life science, biomedical, public health, or related field required; Master's degree (M.S., M.P.H., or equivalent) strongly preferred.
  • Minimum 1 year of hands-on experience in a clinical or academic research setting.
  • Demonstrated experience with IRB submissions and human subjects research regulations
  • Familiarity with IACUC processes and animal research regulatory frameworks
  • Experience contributing to manuscript preparation or grant applications.
  • Strong scientific writing and editing skills with high attention to detail.

This position is intended to support clinical research and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.

NOTE: Position tasks are generally required to be performed in-person at an Emory University location.  Remote work from home day options may be granted at department discretion. Emory reserves the right to change remote work status with notice to employee.

Additional Details

Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: 404-727-9867 (V) | 404-712-2049 (TDD).

Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination.

Employment Type: OTHER

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