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Regulatory Operations Manager Jobs in Georgia (NOW HIRING)

Arclin

Operations Manager

Albany, GA

This position ensures that the plant is operating in compliance with all regulatory and company policies, procedures and regulations. Operations Manager I Job Responsibilities: * Plan, organize and ...

Arclin

Operations Manager

Albany, GA · On-site

This position ensures that the plant is operating in compliance with all regulatory and company policies, procedures and regulations. Operations Manager I Job Responsibilities: * Plan, organize and ...

Arclin

Operations Manager

Albany, GA · On-site

This position ensures that the plant is operating in compliance with all regulatory and company policies, procedures and regulations. Operations Manager I Job Responsibilities: * Plan, organize and ...

Construction Execs

Operations Manager

Suwanee, GA

$120K - $160K/yr

Seeking an Experienced Operations Manager (Industrial or Commercial Construction) Are you an ... regulations and safety standards, mitigating potential risks. - Drive a culture of continuous ...

ServiceMaster

Operations Manager

Tifton, GA · On-site

$50K - $60K/yr

Ensuring that health and safety regulations are followed * Examine financial data and use them to improve profitability, managing budgets, budgetary changes and forecasts * Improve operational ...

PRIORITY ONDEMAND

Operations Manager

Tifton, GA · On-site

The Operations Manager must maintain knowledge of local, state, and federal laws and regulations applicable to ambulance and wheelchair transportation services. He or she maintains relationships with ...

PIVOT Workforce

Operations Manager

Atlanta, GA

$125K - $150K/yr

OPERATIONS MANAGER - MECHANICAL CONTRACTOR LOCATION: Greater Atlanta, GA WHAT YOU WILL BE DOING We ... Stay abreast of industry trends, regulations, and best practices to drive innovation and efficiency.

EoS Fitness

Our Operations Manager, reporting to the District Operations Manager, is responsible for overseeing ... Ensuring compliance with health and safety regulations, maintaining proper certifications, and ...

EoS Fitness

Operations Manager

Folkston, GA

Our Operations Manager, reporting to the District Operations Manager, is responsible for overseeing ... Ensuring compliance with health and safety regulations, maintaining proper certifications, and ...

Gururo

Operations Manager

Atlanta, GA · On-site +1

As the Operations Manager, you will be responsible for overseeing and optimizing various ... industry regulations and standards. * Vendor Management: Oversee relationships with external ...

Boise Cascade

Operations Manager

Auburn, GA · On-site

$75K - $115K/hr

... regulations and legal load requirements. Manage the warehouse function including receipt of ... The Operations Manager manages warehouse, equipment and vehicles, yard and grounds to ensure a safe ...

Boise Cascade Company

Operations Manager

Auburn, GA · On-site

$75K - $115K/yr

... regulations and legal load requirements. Manage the warehouse function including receipt of ... The Operations Manager manages warehouse, equipment and vehicles, yard and grounds to ensure a safe ...

Boise Cascade Company

Operations Manager

Auburn, GA · On-site

$75K - $115K/yr

... regulations and legal load requirements. Manage the warehouse function including receipt of ... The Operations Manager manages warehouse, equipment and vehicles, yard and grounds to ensure a safe ...

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All JobsRegulatory Operations JobsRegulatory Operations Manager JobsRegulatory Operations Manager Jobs in Georgia

Regulatory Operations Manager information

See Georgia salary details

$26.2K

$53.6K

$100.1K

How much do regulatory operations manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for regulatory operations manager in Georgia is $53,581.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,600.00 and $65,400.00 per year, depending on experience, location, and employer.

What does a regulatory operations manager do?

A Regulatory Operations Manager oversees the processes and systems required to ensure an organization complies with all regulatory requirements, especially in highly regulated industries like pharmaceuticals, finance, or healthcare. Their responsibilities often include managing the submission of documents to regulatory agencies, ensuring accurate record-keeping, developing compliance strategies, and coordinating with various internal departments. They play a critical role in maintaining regulatory standards and facilitating timely approvals for product launches or business activities.

What are the key skills and qualifications needed to thrive as a regulatory operations manager?

To thrive as a Regulatory Operations Manager, you need expertise in regulatory compliance, project management, and a relevant degree in life sciences or a related field. Familiarity with electronic document management systems (EDMS), regulatory submission platforms like eCTD, and knowledge of global regulatory requirements are typically required. Strong attention to detail, organizational skills, and effective cross-functional communication set outstanding professionals apart in this role. These competencies are crucial for ensuring timely, accurate regulatory submissions and facilitating seamless collaboration within regulatory and cross-functional teams.

How does a regulatory operations manager collaborate with cross-functional teams to ensure timely regulatory submissions?

A Regulatory Operations Manager works closely with regulatory affairs, clinical, quality assurance, and project management teams to coordinate the preparation, review, and submission of regulatory documents. They serve as a central point of contact, facilitating communication and aligning timelines to ensure all required materials are gathered and compliant with regulatory standards. By organizing regular meetings and utilizing document management systems, they help streamline the submission process and proactively identify and resolve potential bottlenecks.

What is the difference between Regulatory Operations Manager vs Regulatory Affairs Specialist?

AspectRegulatory Operations ManagerRegulatory Affairs Specialist
CredentialsTypically requires a bachelor’s degree in life sciences, regulatory affairs, or related field; certifications like RAC are commonSimilar credentials; often holds a bachelor’s degree and may pursue regulatory certifications
Work EnvironmentManages regulatory processes, documentation, and compliance within organizations, often overseeing teamsFocuses on preparing and submitting regulatory documents, ensuring compliance with regulations
Industry UsageUsed across pharmaceutical, biotech, and medical device companies for operational oversightCommonly found in similar industries, focusing on regulatory submissions and communication with authorities

The Regulatory Operations Manager oversees the regulatory process, managing teams and ensuring compliance, while the Regulatory Affairs Specialist concentrates on preparing submissions and liaising with regulatory agencies. Both roles require similar credentials and are vital in regulated industries, but their focus areas differ slightly.

Is regulatory compliance a stressful job?

Regulatory Operations Managers often find regulatory compliance to be demanding due to strict deadlines, detailed documentation, and the need to stay current with evolving regulations. The role requires strong attention to detail, organizational skills, and the ability to manage multiple priorities, which can contribute to work-related stress.

Is regulatory operations a good career path?

Regulatory operations is a viable career path for professionals interested in compliance, documentation, and process management within regulated industries such as pharmaceuticals, biotech, and healthcare. It often requires strong attention to detail, knowledge of regulatory requirements, and proficiency with tools like document management systems. The role offers opportunities for advancement and specialization, with demand driven by industry regulations and compliance needs.

What are the most commonly searched types of Regulatory Operations jobs in Georgia?

The most popular types of Regulatory Operations jobs in Georgia are:

What are popular job titles related to Regulatory Operations Manager jobs in Georgia?

For Regulatory Operations Manager jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Regulatory Operations Manager jobs in Georgia look for?

The top searched job categories for Regulatory Operations Manager jobs in Georgia are:

What cities in Georgia are hiring for Regulatory Operations Manager jobs?

Cities in Georgia with the most Regulatory Operations Manager job openings:

Regulatory Operations Manager jobs near you
Infographic showing various Regulatory Operations Manager job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 11% Part Time, 1% Temporary, 7% Contract, and 3% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $53,581 per year, or $25.8 per hour.

Regulatory Operations Specialist

St. Joseph's/Candler

Savannah, GA • On-site

$19.28/hr

Full-time

Posted 10 days ago

St. Joseph's/Candler Health System rating

7.0

Company rating: 7.0 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

Job description

  • Position Summary

    • The Research Regulatory Specialist is responsible for coordinating the daily activities associated with supporting the regulatory department at the Nancy N. and J.C. Lewis Cancer & Research Pavilion (LCRP). The individual will perform clerical activities including filing, scanning, faxing and documentation management. The individual will be the upkeep of regulatory documentation associated with pharmaceutical and National Cancer Center (NCI) Central Institutional Review Board (CIRB) and the ADVARRA CIRB as appropriate.  The individual will be responsible for safety reporting, updating the LCRP and Georgia Center for Oncology Research and Education (GA CORE) websites, regulatory meeting minutes, bi-weekly research meeting minutes and assisting the manager and regulatory coordinator with additional research related duties. The successful candidate complies with all SJ/C policies, procedures, departmental guidelines, and applicable laws in the conduct of routine activities and the solution of problems; prepares documents for regulatory review, monitoring and auditing.   

      Ensures that all regulatory documents are in compliance and maintained in accordance with Good Clinical Practice (GCP), Department of Health and Human Services (DHHS), and the Food and Drug Administration (FDA) guidelines.

      Works independently to assure compliance with the requests of sponsors, SJ/C IRB and internal managers as needed.

      Works with Regulatory and Compliance Manager, the Research Regulatory Coordinator- Lead and the Clinical Research Coordinator (CRC) in scheduling and conducting monitoring visits, responding to monitoring, audit reports and additional research protocol duties as needed.

      Maintains sponsor, investigator and research personnel regulatory communication.

  • Education
    • Associate's Degree - Required
    • Bachelor's Degree - Preferred
  • Experience
    • 1-2 Years of General Healthcare or Legal experience - Preferred
  • License & Certification
    • Good Clinical Practice (GCP) and Human Protections Training  - Preferred
  • Core Job Functions
    • Assist in maintaining regulatory master files for each clinical trial and assist in preparing documents for IRB and/or sponsor review.
    • Ensure all study specific Financial Disclosure Forms (FDFs), annual FDFs and safety reports are prepared, filed, completed, and submitted accurately in a timely manner. Other trial-related documents are processed in a timely manner. Responsible for delivery and pickup of regulatory documents between site locations and retrieving provider and staff signatures.
    • Maintain research staff trainings and credentialing using a tracking system.
    • Coordinate various forms of communication, including but not limited to telephone, email and responding to the Regulatory & Compliance Manager and Regulatory Coordinator. Accurately managing documents in accordance with appropriate clinical trial. Responsible for ordering supplies and scheduling the conference room for the office.
    • Maintain historical and current documents for clinical trials utilizing both CREDIT & Florence software and others as appropriate. Maintain the LCRP website and GA CORE website to ensure all active trials are visible to the community. Ensure appropriate research sites are activated within the CREDIT system. 

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