ZipRecruiter

Log In

1

Clinical Research Regulatory Jobs in Decatur, GA

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Maintain regulatory compliance with FDA, ICH-GCP, and institutional guidelines * Coordinate with ... Previous clinical research experience * CCRP (Certified Clinical Research Professional) or ACRP ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Maintain regulatory compliance with FDA, ICH-GCP, and institutional guidelines * Coordinate with ... Previous clinical research experience * CCRP (Certified Clinical Research Professional) or ACRP ...

next page

Showing results 1-20

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 Aug 21, 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 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.

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 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 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 August 2026, with employment types broken down into 3% As Needed, 69% Full Time, 20% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $83,517 per year, or $40.2 per hour.

Clinical Research Nurse

Alcanza Clinical Research

Decatur, GA • On-site

Other

Medical, Dental, Vision, Life, Retirement

Re-posted 3 hours ago

Job description

Clinical Research Nurse
Department: Operations
Employment Type: Full Time
Location: Accel Research Sites - Decatur, GA
Reporting To: Benoit Tete
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Research Nurse works to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.
Key Responsibilities
Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
  • Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines:
    • Screening of patients for study enrollment;
    • Patient consents;
    • Patient follow-up visits;
    • Documenting in source clinic charts;
    • Entering data in EDC and answers queries;
    • Obtaining vital signs and ECGs;
    • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
    • Performing procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.
    • Requesting and tracking medical record requests;
    • Updating and maintaining logs, chart filings;
    • Maintaining & ordering study specific supplies;
    • Scheduling subjects for study visits and conducts appointment reminders;
    • Building/updating source as needed;
    • Conducting monitoring visits and resolves issues as needed in a timely manner;
    • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
o Filing SAE/Deviation reports to Sponsor and IRB as needed;
o Documenting and reporting adverse events;
o Reporting non-compliance to appropriate staff in timely manner;
o Maintaining positive and effective communication with clients and team members;
o Always practicing ALCOAC principles with all documentation;
  • Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
  • May set up, train and maintain all technology needed for studies.
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • Maintaining confidentiality of patients, customers and company information, and;
  • Performing all other duties as requested or assigned.
Skills, Knowledge and Expertise
Minimum Qualifications: A Bachelor's degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required. An active, unrestricted RN license, in state of work location, is required. BLS certification required. Bi-lingual (English / Spanish) proficiency is a plus.
Required Skills:
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Proficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required.
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

Apply