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Remote Regulatory Affairs Intern Jobs (NOW HIRING)

YO AI Labs

Regulatory Affairs Expert - Remote

Dallas, TX · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

YO AI Labs

Regulatory Affairs Expert - Remote

Miami, FL · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

YO AI Labs

Regulatory Affairs Expert - Remote

Chicago, IL · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

YO AI Labs

Regulatory Affairs Expert - Remote

Phoenix, AZ · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

YO AI Labs

Regulatory Affairs Expert - Remote

Atlanta, GA · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

YO AI Labs

Regulatory Affairs Expert - Remote

Boston, MA · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

YO AI Labs

Regulatory Affairs Expert - Remote

Seattle, WA · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

YO AI Labs

Regulatory Affairs Expert - Remote

Austin, TX · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

Oscar Health

Analyst, Regulatory Affairs

Atlanta, GA · 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 ...

Oscar Health

Analyst, Regulatory Affairs

Dallas, TX · 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: Dallas, TX. You will be fully remote ...

YO AI Labs

Regulatory Affairs Expert - Remote

Seattle, WA · Remote

$50 - $80/hr

Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating ...

New

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Remote Regulatory Affairs Intern information

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

As of Aug 13, 2026, the average hourly pay for remote regulatory affairs intern in the United States is $17.04, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What is a remote regulatory affairs intern?

Remote Regulatory Affairs Interns are students or recent graduates who support regulatory affairs teams from a remote location, usually working online. Their main responsibilities include assisting with the preparation and review of regulatory documents, researching relevant laws and regulations, and helping ensure that products comply with government requirements. These interns gain valuable experience in regulatory processes within industries like pharmaceuticals, medical devices, or biotechnology while working flexibly from home or another remote setting.

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

To thrive as a Remote Regulatory Affairs Intern, you need a strong understanding of regulatory guidelines, attention to detail, and typically a background in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and sometimes certifications like RAC (Regulatory Affairs Certification) are beneficial. Excellent written communication, organizational skills, and the ability to work independently are standout soft skills in this role. These competencies are crucial for ensuring compliance, timely submissions, and effective remote collaboration within regulatory teams.

What are the typical responsibilities of a remote regulatory affairs intern, and how do they contribute to the team?

As a Remote Regulatory Affairs Intern, you will support the regulatory team by assisting with the preparation and review of regulatory documents, maintaining compliance records, and conducting research on relevant regulations and guidelines. You may help track submission deadlines, update databases, and coordinate with cross-functional teams, such as quality assurance and product development, to gather necessary information. Your contributions are essential in ensuring that products meet all regulatory requirements, which helps facilitate timely approvals and market access.
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Remote Regulatory Affairs Intern jobs near you
Infographic showing various Remote Regulatory Affairs Intern job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 9% Part Time, and 3% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $35,436 per year, or $17 per hour.

Remote Regulatory Affairs contractor

Globalchannelmanagement

Atlanta, GA • Remote

$99 - $100/hr

Full-time

Re-posted 17 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