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Remote Biotech Regulatory Affairs Jobs in Decatur, GA

Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI ... Required Qualifications * 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech ...

Analyst, Regulatory Affairs

Atlanta, GA ยท Remote

$28.30 - $37.15/hr

  • Medical

  • PTO

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first ... This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote ...

Analyst, Regulatory Affairs

Atlanta, GA ยท Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first ... This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote ...

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help ...

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help ...

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help ...

Compliance Officers

Atlanta, GA ยท Remote

$50 - $70/hr

Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory ...

Compliance Officers

Sandy Springs, GA ยท Remote

$50 - $70/hr

Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory ...

Compliance Officers

South Fulton, GA ยท Remote

$50 - $70/hr

Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory ...

LIMS SME/Business Analyst

Atlanta, GA ยท Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Regulatory Affairs (ORA). The duties for this position is as follows: Work with end users and ... This is a remote position so the candidate can live anywhere in the USA. The position will require ...

Regulatory & Clinical Specialist

Atlanta, GA ยท Remote

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... affairs or a Ph.D. with at least 3 years of experience Location & Travel Requirements ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

VP, State Government Affairs

Atlanta, GA ยท On-site +1

$220K - $275K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Anticipate evolving regulatory trends, influencing policy outcomes before they crystallize, and ... S. and are willing to consider remote candidates. #LI-Remote Working at PrizePicks: The typical ...

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Showing results 1-20

Remote Biotech Regulatory Affairs information

See Decatur, GA salary details

$18

$38

$61

How much do remote biotech regulatory affairs jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for remote biotech regulatory affairs in Decatur, GA is $38.63, according to ZipRecruiter salary data. Most workers in this role earn between $30.96 and $45.77 per hour, depending on experience, location, and employer.

What is a remote biotech regulatory affairs professional?

Remote Biotech Regulatory Affairs professionals are specialists who ensure that biotechnology products and processes comply with all relevant regulations and laws. Working remotely, they manage documentation, submissions, and communications with regulatory agencies to facilitate product approvals. They play a key role in keeping companies compliant with evolving guidelines, such as those from the FDA or EMA, while working from locations outside traditional offices. Their work ensures that new biotech products are safe, effective, and legally marketable.

How does a remote biotech regulatory affairs professional typically collaborate with cross-functional teams while working offsite?

In a remote Biotech Regulatory Affairs role, professionals frequently interact with teams such as research, clinical, quality assurance, and legal through virtual meetings and collaborative platforms. Regular communication is essential to coordinate submission timelines, ensure documentation accuracy, and address regulatory concerns promptly. Successful remote professionals are adept at using project management tools and maintaining proactive communication to bridge any gaps caused by physical distance. This collaborative approach helps ensure that regulatory requirements are met efficiently and that projects progress smoothly.

What are the key skills and qualifications needed to thrive as a remote biotech regulatory affairs professional, and why are they important?

To thrive as a Remote Biotech Regulatory Affairs professional, you need a strong background in biological sciences or related fields, regulatory knowledge, and experience with drug or device development, often supported by a relevant degree or advanced certification such as RAC. Familiarity with regulatory submission systems (e.g., eCTD), FDA/EMA guidelines, and document management platforms is essential. Exceptional attention to detail, written communication, and cross-functional collaboration skills set standout professionals apart in this field. These competencies ensure regulatory compliance, smooth product approvals, and effective coordination across global teams in a highly regulated environment.

What is the difference between Remote Biotech Regulatory Affairs vs Remote Biotech Quality Assurance?

AspectRemote Biotech Regulatory AffairsRemote Biotech Quality Assurance
Primary FocusRegulatory compliance, submissions, and interactions with authoritiesProduct quality, standards, and process validation
Required CredentialsLife sciences degree, regulatory certifications (e.g., RAC)Life sciences degree, quality management certifications (e.g., CQE)
Work EnvironmentCollaborates with regulatory agencies, cross-functional teamsWorks with manufacturing, quality control, and validation teams
Industry UsageCommon in biotech, pharma, and medical device companiesPrevalent in biotech, pharma, and manufacturing sectors

Remote Biotech Regulatory Affairs focuses on ensuring products meet regulatory standards and managing agency submissions, while Remote Biotech Quality Assurance emphasizes maintaining product quality and compliance through internal processes. Both roles require similar credentials and often collaborate but serve distinct functions within biotech companies.

What job categories do people searching Remote Biotech Regulatory Affairs jobs in Decatur, GA look for?

The top searched job categories for Remote Biotech Regulatory Affairs jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Remote Biotech Regulatory Affairs jobs?

Cities near Decatur, GA with the most Remote Biotech Regulatory Affairs job openings:

Infographic showing various Remote Biotech Regulatory Affairs job openings in Decatur, GA as of June 2026, with employment types broken down into 1% As Needed, 42% Full Time, 42% Part Time, 1% Temporary, and 14% Contract. Highlights an 48% Physical, 3% Hybrid, and 49% Remote job distribution, with an average salary of $80,359 per year, or $38.6 per hour.

Regulatory Affairs Expert - Remote

YO AI Labs

Atlanta, GA โ€ข Remote

$50 - $80/hr

Full-time

Posted 7 days ago


Job description

Job Title: Regulatory Affairs Specialist
Location: Remote
Job Type: ContractJob Description

We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating regulatory documentation. The role involves assessing clinical documents, ensuring compliance with regulatory guidelines, identifying inconsistencies, and providing clear, evidence-based feedback to improve AI-generated regulatory content.

Key Responsibilities
  • Review and evaluate clinical and regulatory documentation.

  • Assess regulatory submissions and responses for accuracy and compliance.

  • Ensure adherence to ICH guidelines and CTD/eCTD requirements.

  • Identify regulatory risks, inconsistencies, and unsupported claims.

  • Prepare structured, guideline-based written feedback.

Required Qualifications
  • 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry.

  • Experience with clinical submissions, regulatory documentation, and health authority interactions.

  • Strong knowledge of ICH guidelines and CTD/eCTD structure.

  • Excellent analytical, critical thinking, and written communication skills.

  • Degree in Life Sciences, Pharmacy, Medicine, or a related field.