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Clinical Research Regulatory Assistant Jobs in Decatur, GA

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Clinical Research Coordinator

Johns Creek, GA

$22.50 - $30/hr

Clinical Research Coordinator ICON is a global healthcare intelligence and clinical research ... Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure ...

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 ... Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure ...

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All JobsClinical Research Regulatory JobsClinical Research Regulatory Assistant JobsClinical Research Regulatory Assistant Jobs in Decatur, GA

Clinical Research Regulatory Assistant information

See Decatur, GA salary details

$7

$22

$45

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

As of Jul 30, 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 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 key skills and qualifications needed to thrive as a Clinical Research Regulatory Assistant, and why are they important?

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 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 Regulatory Assistant jobs near you

Regulatory Affairs Specialist (North America)

Alimentiv

Atlanta, GA • Remote

Full-time

Posted 17 days ago

Job description

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies, and the research, review and reporting on applicable global regulations and requirements. Develop stakeholder tools, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities.  Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines.  May be required to coach peers and/or provide input for staff performance reviews. 
Unit Management
  • Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
  • Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.
Client Services
  • As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance guidance and support to project stakeholders.
  • Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.
Regulatory Strategy Development
  • Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
  • Participate in specialized conferences/meetings to increase knowledge as needed.
Project Support
  • Regularly respond to registration requests and work with project teams to identify regulatory requirements.
  • Assist in the preparation of regulatory submissions and support summaries.
  • Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.
Qualifications
  • Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
  • The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
  • Fluency in English and Spanish (written and verbal) required.
Working Conditions
  • Home-based
  • *Accommodations for job applicants with disabilities are available upon request.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.