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Clinical Research Regulatory 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 Jobs in Decatur, GA

Clinical Research Regulatory information

See Decatur, GA salary details

$11

$40

$68

How much do clinical research regulatory jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for clinical research regulatory in Decatur, GA is $40.15, according to ZipRecruiter salary data. Most workers in this role earn between $28.17 and $51.39 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Clinical Research Regulatory position, and why are they important?

To thrive as a Clinical Research Regulatory professional, you need a solid understanding of clinical research processes, regulatory requirements, and compliance standards, often backed by a degree in life sciences or a related field. Familiarity with regulatory submission systems (such as IRB portals), document management tools, and certifications like RAC (Regulatory Affairs Certification) are highly valued. Detail orientation, effective communication, and problem-solving abilities are vital for managing complex documentation and coordinating with diverse teams. These skills enable safe, compliant, and efficient clinical research studies in a highly regulated environment.

What is a Clinical Research Regulatory job?

A Clinical Research Regulatory job involves ensuring that clinical trials comply with regulatory requirements, ethical guidelines, and institutional policies. Professionals in this role prepare and submit regulatory documents, liaise with regulatory agencies, and maintain compliance throughout the study. They work closely with clinical teams, sponsors, and ethics committees to ensure research integrity and patient safety. Strong knowledge of FDA regulations, ICH-GCP guidelines, and institutional review board (IRB) processes is essential.

What are some common challenges faced by Clinical Research Regulatory professionals?

Clinical Research Regulatory professionals often face the challenge of navigating complex and evolving regulations while ensuring timely and accurate submission of documentation for clinical trials. Keeping up-to-date with global regulatory changes and managing tight deadlines can be demanding, especially when supporting multiple studies simultaneously. Strong collaboration with clinical, legal, and quality assurance teams is essential to address compliance issues and resolve ambiguities. Adapting to shifting priorities and maintaining meticulous attention to detail are also crucial for success in this role.

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 jobs in Decatur, GA? For Clinical Research Regulatory jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Regulatory jobs in Decatur, GA look for? The top searched job categories for Clinical Research Regulatory jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Research Regulatory jobs? Cities near Decatur, GA with the most Clinical Research Regulatory job openings:
Clinical Research Regulatory jobs near you
Infographic showing various Clinical Research Regulatory job openings in Decatur, GA as of July 2026, with employment types broken down into 2% As Needed, 76% Full Time, 16% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,517 per year, or $40.2 per hour.

Regulatory Affairs Specialist (North America)

Alimentiv

Atlanta, GA • Remote

Full-time

Posted 13 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.