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Regulatory Affairs Contractor Jobs (NOW HIRING)

micro1 AI

Regulatory Affairs Specialist

Roanoke, VA · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Billings, MT · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Mckinney, TX · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Tempe, AZ · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Suffolk, VA · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

League City, TX · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Richardson, TX · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Baltimore, MD · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Boston, MA · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Little Rock, AR · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Boulder, CO · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Clarksville, TN · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Cincinnati, OH · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Fort Wayne, IN · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Everett, WA · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Evansville, IN · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Miami Gardens, FL · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Orlando, FL · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

Pittsburgh, PA · Remote

$50 - $70/hr

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 ...

micro1 AI

Regulatory Affairs Specialist

South Fulton, GA · Remote

$50 - $70/hr

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 ...

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Regulatory Affairs Contractor information

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$86

How much do regulatory affairs contractor jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for regulatory affairs contractor in the United States is $56.97, according to ZipRecruiter salary data. Most workers in this role earn between $42.07 and $66.59 per hour, depending on experience, location, and employer.

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

To thrive as a Regulatory Affairs Contractor, you need a solid understanding of regulatory guidelines, submission processes, and compliance requirements, often supported by a degree in life sciences or a related field. Familiarity with electronic submission systems (such as eCTD), regulatory databases, and certifications like RAC are highly valued. Strong attention to detail, effective communication, and project management skills help you navigate complex regulations and coordinate across departments. These skills ensure timely approvals, minimize compliance risks, and support successful product market entry.

What are some typical challenges faced by regulatory affairs contractors when managing submissions across multiple regions?

Regulatory Affairs Contractors often encounter challenges related to varying regulatory requirements, documentation standards, and submission timelines across different countries or regions. Navigating these complexities requires strong attention to detail, up-to-date knowledge of global regulations, and effective communication with cross-functional teams. Contractors must frequently coordinate with local affiliates, adapt to shifting regulatory landscapes, and ensure timely, compliant submissions—making adaptability and organizational skills essential for success in this role.

What is the difference between Regulatory Affairs Contractor vs Regulatory Affairs Specialist?

AspectRegulatory Affairs ContractorRegulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences or related field; certifications like RAC are commonSame as contractor; often holds similar certifications and degrees
Work EnvironmentContract-based, project-specific, often freelance or temporary rolesFull-time, permanent roles within companies or organizations
Employer & Industry UsageUsed by companies seeking flexible regulatory support, especially during product launches or auditsEmployed by companies to ensure ongoing regulatory compliance and submissions

While both roles require similar credentials and work within the same industry, a Regulatory Affairs Contractor typically works on a temporary, project basis, providing specialized expertise as needed. In contrast, a Regulatory Affairs Specialist is a full-time employee responsible for ongoing regulatory activities within an organization.

What is a regulatory affairs contractor?

Regulatory Affairs Contractors are professionals hired on a temporary or project basis to support organizations in managing regulatory compliance and submissions. They help ensure that products, such as pharmaceuticals, medical devices, or food items, meet all governmental regulations and industry standards. These contractors often prepare documentation, interact with regulatory agencies, and provide strategic advice on regulatory requirements. Their expertise is especially valuable during product development, market entry, or when navigating changes in regulations.
More about Regulatory Affairs Contractor jobs
What cities are hiring for Regulatory Affairs Contractor jobs? Cities with the most Regulatory Affairs Contractor job openings:
What states have the most Regulatory Affairs Contractor jobs? States with the most job openings for Regulatory Affairs Contractor jobs include:
What job categories do people searching Regulatory Affairs Contractor jobs look for? The top searched job categories for Regulatory Affairs Contractor jobs are:
Regulatory Affairs Contractor jobs near you
Infographic showing various Regulatory Affairs Contractor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, and 4% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $118,493 per year, or $57 per hour.

Regulatory Affairs Specialist

micro1 AI

Roanoke, VA • Remote

$50 - $70/hr

Part-time

Posted 4 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).

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