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Clinical Research Regulatory Jobs in Decatur, GA

Clinical Research Coordinator II

Decatur, GA

$23.75 - $31.50/hr

Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. * Maintain effective relationships with study participants and other care Access Research ...

Clinical Research Coordinator II

Decatur, GA · On-site

$23.75 - $31.50/hr

Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. * Maintain effective relationships with study participants and other care Access Research ...

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 ...

Clinical Research Coordinator II

Decatur, GA

$23.75 - $31.50/hr

Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.  * Maintain effective relationships with study participants and other care Access Research ...

... GCP, ICH, HIPAA, FDA Regulations and SOPs. Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies.

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH ...

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH ...

Showing results 41-60

Clinical Research Regulatory information

See Decatur, GA salary details

$11

$40

$68

How much do clinical research regulatory jobs pay per hour?

As of Aug 8, 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 clinical research regulatory?

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?

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.

Is clinical research regulatory an entry level job?

Clinical research regulatory roles can be entry-level, especially for positions such as Regulatory Assistants or Coordinators, which often require a bachelor's degree and some familiarity with regulations like GCP or FDA guidelines. However, more senior roles typically require additional experience or specialized certifications, such as RAC (Regulatory Affairs Certification).

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 does a clinical research regulatory specialist do?

A clinical research regulatory specialist ensures that clinical trials comply with government regulations and guidelines. They prepare and review documentation, submit regulatory approvals, and coordinate with oversight agencies to facilitate trial approval and conduct. Strong knowledge of regulations such as FDA or EMA requirements and attention to detail are essential 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 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:
Infographic showing various Clinical Research Regulatory job openings in Decatur, GA as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% 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.

Clinical Research Coordinator I-School of Medicine, Georgia CTSA

Emory University

Atlanta, GA • On-site

$23.50 - $31.50/hr

Full-time

Re-posted 6 days ago


Emory Healthcare rating

7.7

Company rating: 7.7 out of 10

Based on 217 frontline employees who took The Breakroom Quiz

161st of 887 rated healthcare providers


Job description

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.


The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.

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:

  • Prior experience in clinical research, healthcare, or patient-facing settings.
  • Familiarity with clinical research regulations, IRB submissions, informed consent, and Good Clinical Practice guidelines.
  • Experience with electronic medical records, REDCap, OnCore, eIRB, or other clinical research databases.
  • Strong organizational skills and attention to detail.
  • Excellent written and verbal communication skills.
  • Ability to work effectively with study participants, investigators, sponsors, and clinical teams. 
  • Ability to manage multiple tasks and meet deadlines in a fast-paced clinical research environment.

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.


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.


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