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Remote Regulatory Intelligence Jobs (NOW HIRING)

Altimmune

Director, US Regulatory Affairs

Morristown, NJ · On-site +1

$154K - $204K/yr

Depending upon location, this role will be hybrid or remote and will require some travel as ... intelligence * Attends relevant FDA meetings and interfaces with regulatory/competent authorities ...

Precision for Medicine

Regulatory Manager

Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to ... proficiency #LI-Remote Precision is required by law in some states or cities to include a ...

Precision Medicine Group

Regulatory Manager

Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to ... proficiency #LI-Remote Precision is required by law in some states or cities to include a ...

Precision for Medicine

Regulatory Manager

Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to ... proficiency #LI-Remote Precision is required by law in some states or cities to include a ...

Oath

Global Regulatory Affairs Lead

Vacaville, CA · Remote

Regulatory Intelligence: Monitor, interpret, and communicate changes in the global regulatory ... Home-based / Remote (USA-based preferred for proximity to North American R&D and commercial ...

Eisai

Director, Global Regulatory Affairs

$153K - $202K/yr

... regulatory intelligence concerning competitor products. * Communicate regulatory issues to ... We will consider remote candidates who are unable to regularly work in our Nutley, NJ office * Must ...

Travere

Manager, Regulatory Affairs Strategy

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Contribute to regulatory intelligence efforts by evaluating emerging regulations, guidance ...

Cardinal Health

This is a remote position, and the ideal candidate will be located near or willing to travel to ... Maintain regulatory intelligence, identify compliance risks, and develop mitigation and resolution ...

Travere

Director, Regulatory Affairs Strategy

$153K - $202K/yr

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Regulatory Intelligence & Compliance * Monitor evolving global regulatory requirements, guidance ...

Travere

Director, Regulatory Affairs Strategy

San Diego, CA · On-site +1

$159K - $210K/yr

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... Regulatory Intelligence & Compliance * Monitor evolving global regulatory requirements, guidance ...

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Remote Regulatory Intelligence information

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How much do remote regulatory intelligence jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for remote regulatory intelligence in the United States is $50.06, according to ZipRecruiter salary data. Most workers in this role earn between $34.86 and $51.92 per hour, depending on experience, location, and employer.

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

AspectRemote Regulatory IntelligenceRegulatory Affairs Specialist
CredentialsTypically requires degrees in life sciences, certifications in regulatory affairs or intelligenceRequires degrees in life sciences, certifications like RAC or RAPS
Work EnvironmentPrimarily remote, focused on research and analysisOften office-based or hybrid, involved in compliance and submission processes
Industry UsageUsed in pharmaceutical, biotech, and medical device sectors for monitoring regulationsInvolved in preparing and submitting regulatory documents to authorities

Remote Regulatory Intelligence focuses on gathering and analyzing regulatory information remotely, while Regulatory Affairs Specialists handle compliance, submissions, and communication with authorities. Both roles require regulatory knowledge but differ in daily tasks and work settings.

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Remote Regulatory Intelligence jobs near you
Infographic showing various Remote Regulatory Intelligence 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 $104,126 per year, or $50.1 per hour.

Remote Regulatory Affairs contractor

Globalchannelmanagement

Atlanta, GA • Remote

$99 - $100/hr

Full-time

Re-posted 28 days ago

Job description

Remote Regulatory Affairs contractor requires:

  • Bachelor's degree in engineering, life sciences, regulatory affairs, legal or a related field
  • 5-10 years+ of global medical device regulatory experience
  • Proven experience preparing, writing and submitting FDA 510k submissions (end to end)
  • Experience with ophthalmic devices, capital equipment, diagnostic devices, software in medical devices, cybersecurity
  • Strong working knowledge of:
    • FDA regulations (21 Parts 807, 820)
    • FDA guidance documents and eStar requirements
    • Experience with Canadian regulations, EU MDR (2017/745) including Class lla, Tech docs Annex ll/lll
  • Demonstrated ability to work independently as a contractor in a fast-paced environment
  • Experience filing medical device submissions in China and other countries
  • Experience with audiology devices
  • Experience with artificial-intelligence enabled devices
  • Strong technical writing and documentation skills
  • Ability to translate complex technical information into regulatory submissions
  • Detail-oriented with strong organization skills
  • Effective communicator across technical and non-technical stakeholders
  • Ability to manage multiple deliverables and timelines

DUTIES:

  • FDA 510(k) submission
  • Conduct comprehensive review of technical documentation (design controls, V&V, risk, labeling, clinical evidence, and software as applicable) to ensure completeness, quality, and regulatory compliance
  • Perform detailed regulatory gap assessments against FDA requirements (21 CFR Parts 807, 820, and applicable FDA guidance documents)
  • Author, compile and deliver a complete 510k submission, including preparation in FDA eSTAR format,
  • Lead submission lifecycle activities, including:
    • Acceptance Review support (RTA readiness)
    • Substantive Review coordination
    • Drafting and submission of responses to FDA requests for Additional Information, Interactive review communications
    • Updating submission content and modules as required
  • Interface cross-functionally to incorporate Business inputs and ensure alignment throughout the review process.
  • Provide regulatory leadership through FDA clearance.
  • EU MDR Technical Documentation Support
  • Conduct EU MDR readiness assessment aligned with Notified Body expectations and conformity assessment requirements.
  • Perform critical review and gap analysis of EU MDR technical file
  • Provide targeted recommendations to ensure audit-readiness and Notified Body acceptance
  • Lead or support submission to obtain CE Mark
  • Health Canada submission
  • Global Regulatory Strategy and Advisory