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Regulatory Affairs Manager Remote Jobs in Racine, WI

micro1 AI

Regulatory Affairs Specialist

Kenosha, 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

Milwaukee, 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

Compliance Officers

Kenosha, WI · 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 ...

micro1 AI

Compliance Officers

Milwaukee, WI · 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 ...

SERVE YOU RX

Compliance Analyst I

Milwaukee, WI · On-site +1

... Regulatory Affairs to meet company goals and objectives related to corporate compliance. This ... This position is open to remote. What You'll Do: As the Compliance Analyst , you will: * Research ...

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Regulatory Affairs Manager Remote information

See Racine, WI salary details

$27

$53

$81

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

As of Aug 19, 2026, the average hourly pay for regulatory affairs manager remote in Racine, WI is $53.42, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $62.45 per hour, depending on experience, location, and employer.

What does a regulatory affairs manager do when working remotely?

A Regulatory Affairs Manager working remotely is responsible for ensuring that their company's products comply with all relevant regulations and standards set by governmental and regulatory bodies. They prepare and submit documentation, monitor changes in regulations, and communicate with regulatory agencies to facilitate product approvals or renewals. While remote, they use digital tools to collaborate with internal teams, manage compliance projects, and stay updated on industry changes. Their work ensures that products remain in the market legally and safely.

What are the key skills and qualifications needed to thrive as a regulatory affairs manager working remotely?

To excel as a Regulatory Affairs Manager (Remote), you need a deep understanding of regulatory guidelines, compliance procedures, and industry standards, typically supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and certifications like RAC (Regulatory Affairs Certification) are highly valuable. Outstanding organizational skills, attention to detail, and strong communication abilities help you effectively interpret regulations and collaborate across teams. These competencies ensure products meet legal requirements efficiently, minimizing risks and facilitating successful market access.

How does a regulatory affairs manager working remotely typically collaborate with cross-functional teams to ensure compliance?

As a remote Regulatory Affairs Manager, you will regularly interact with cross-functional teams such as R&D, Quality Assurance, Clinical, and Marketing through virtual meetings, email, and collaborative project management tools. Effective communication and proactive coordination are key, as you may need to clarify regulatory requirements, review submission documents, and provide compliance guidance across different time zones. Building strong relationships and maintaining clear documentation helps facilitate seamless collaboration, ensuring all stakeholders are aligned on regulatory expectations and deadlines.

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

AspectRegulatory Affairs Manager RemoteRegulatory Affairs Specialist
CredentialsBachelor's degree, often advanced certifications (RAC)Bachelor's degree, some certifications preferred
Work EnvironmentRemote, managerial oversight, strategic planningRemote or on-site, focused on document preparation and compliance
Industry UsageUsed across pharmaceutical, biotech, medical device companiesCommon in similar industries, often reporting to managers
Search & Comparison IntentUnderstanding managerial roles and responsibilitiesFocus on entry to mid-level regulatory tasks

The Regulatory Affairs Manager Remote oversees regulatory strategies and compliance at a managerial level, often requiring advanced certifications. The Regulatory Affairs Specialist handles specific regulatory tasks, such as preparing documentation and ensuring compliance, typically with less managerial responsibility. Both roles are essential in regulated industries like pharma and biotech, with the manager focusing on strategy and leadership, while the specialist executes detailed regulatory activities.

What job categories do people searching Regulatory Affairs Manager Remote jobs in Racine, WI look for?

The top searched job categories for Regulatory Affairs Manager Remote jobs in Racine, WI are:

What cities near Racine, WI are hiring for Regulatory Affairs Manager Remote jobs?

Cities near Racine, WI with the most Regulatory Affairs Manager Remote job openings:

Regulatory Affairs Manager Remote jobs near you

Regulatory Affairs Specialist

micro1 AI

Kenosha, WI • 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).

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