ZipRecruiter

Log In

2

Remote Biomedical Regulatory Affairs Jobs (NOW HIRING)

micro1 AI

Regulatory Affairs Specialist

Waterbury, CT · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Portland, OR · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Nampa, ID · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Yuma, AZ · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Wichita Falls, TX · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Mcallen, TX · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Washington, DC · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Tampa, FL · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Gresham, OR · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Greensboro, NC · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Hillsboro, OR · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Madison, WI · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Independence, MO · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Columbus, GA · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Rockford, IL · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Rio Rancho, NM · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Shreveport, LA · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Detroit, MI · Remote

$50 - $70/hr

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 ...

previous page

Showing results 41-60

All Jobsremote JobsGovernment JobsGovernment Services JobsRegulatory Affairs Specialist JobsRemote Biomedical Regulatory Affairs Jobs

Remote Biomedical Regulatory Affairs information

See salary details

$18

$39

$62

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

As of Aug 20, 2026, the average hourly pay for remote biomedical regulatory affairs in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

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

AspectRemote Biomedical Regulatory AffairsRemote Biomedical Quality Assurance
Required credentialsLife sciences degree, regulatory certifications (e.g., RAC)Quality management certifications (e.g., CQE, ISO auditor)
Work environmentCollaborates with regulatory agencies, documentation reviewEnsures product quality, audits, compliance checks
Employer usagePharmaceutical, biotech, medical device companiesManufacturers, medical device firms, healthcare organizations
Search intentRegulatory submissions, compliance strategiesProduct quality, process improvements

Remote Biomedical Regulatory Affairs focuses on navigating regulatory requirements and submissions, while Remote Biomedical Quality Assurance emphasizes maintaining product quality and compliance through audits and process controls. Both roles are essential in the biomedical industry and often overlap but serve distinct functions.

More about Remote Biomedical Regulatory Affairs jobs

What cities are hiring for Remote Biomedical Regulatory Affairs jobs?

Cities with the most Remote Biomedical Regulatory Affairs job openings:

What are the most commonly searched types of Biomedical Regulatory Affairs jobs?

The most popular types of Biomedical Regulatory Affairs jobs are:

What states have the most Remote Biomedical Regulatory Affairs jobs?

States with the most job openings for Remote Biomedical Regulatory Affairs jobs include:

What job categories do people searching Remote Biomedical Regulatory Affairs jobs look for?

The top searched job categories for Remote Biomedical Regulatory Affairs jobs are:

Remote Biomedical Regulatory Affairs jobs near you
Infographic showing various Remote Biomedical Regulatory Affairs job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 86% Full Time, 9% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Regulatory Affairs Specialist

micro1 AI

Waterbury, CT • Remote

$50 - $70/hr

Part-time

Posted 16 days ago

Job description

Role Title: 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 documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review evaluation tasks inspired by real-world agency requests and sponsor response threads, determining if drafted responses meet regulatory expectations.
  2. Apply expert judgment to review clinical documentation, assessing whether conclusions are substantiated, commitments are properly scoped, and records can withstand regulatory scrutiny.
  3. Distinguish between substantively adequate and superficially polished responses, articulating clear rationales for any deficiencies.
  4. Assess consistency across comprehensive document sets, identifying unsupported or conflicting claims within or between documents.
  5. Provide structured, well-reasoned written feedback grounded in applicable regulatory guidelines rather than subjective impressions.
  6. Collaborate asynchronously and communicate complex regulatory concepts clearly in both written and verbal form.


Preferred Qualifications

  1. 5+ years of direct regulatory affairs experience at a sponsor, CRO, or consultancy, with responsibility for clinical submissions.
  2. Documented experience drafting or leading responses to health authority information requests, particularly for ongoing regulatory filings.
  3. Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada).
  4. Proven ability to critically read clinical or safety documents to identify regulatory risks, unsupported statements, and potential reviewer concerns.
  5. Exceptional written communication skills, with the capability to convey regulatory reasoning clearly, concisely, and defensibly.
  6. Degree in life sciences, pharmacy, medicine, or a related field; RAC certification is an advantage.
  7. Experience engaging with multiple regions or agencies, prior health authority reviewer/assessor background, or familiarity with AI-assisted regulatory tools (all considered valuable).

Apply