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Remote Regulatory Affairs Internship Jobs in Decatur, GA

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

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 ...

Vensure Employer Services

Be Seen First

Regulatory Manager / Sr. Regulatory Manager - Remote (US)

Atlanta, GA · Remote

$80K - $100K/yr

Strong background in regulatory affairs within food, supplements, cosmetics, or OTC products ... Remote work flexibility * Professional development opportunities * Exposure to diverse industries ...

New

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · Remote

$85K - $95K/yr

... affairs or a Ph.D. with at least 3 years of experience Location & Travel Requirements ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

Medela

Manager, Medical Affairs Operations

Atlanta, GA · On-site +1

$130K/yr

Partner cross-functionally with Medical Affairs, Clinical, Regulatory, and Marketing teams to ... McHenry, IL (3 days in-office and 2 days remote) * Full-time | Exempt Why Join Medela? At Medela ...

New

PrizePicks

VP, State Government Affairs

Atlanta, GA · On-site +1

$220K - $275K/yr

Anticipate evolving regulatory trends, influencing policy outcomes before they crystallize, and ... S. and are willing to consider remote candidates. #LI-Remote Working at PrizePicks: The typical ...

LabAnswer

LIMS SME/Business Analyst

Atlanta, GA · Remote

... Regulatory Affairs (ORA). The duties for this position is as follows: Work with end users and ... This is a remote position so the candidate can live anywhere in the USA. The position will require ...

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Remote Regulatory Affairs Internship information

See Decatur, GA salary details

$15

$33

$142

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

As of Jul 29, 2026, the average hourly pay for remote regulatory affairs internship in Decatur, GA is $33.78, according to ZipRecruiter salary data. Most workers in this role earn between $21.83 and $25.58 per hour, depending on experience, location, and employer.

What is a Remote Regulatory Affairs Internship job?

A Remote Regulatory Affairs Internship is a temporary, often entry-level position where interns gain hands-on experience in regulatory compliance, documentation, and policies related to pharmaceuticals, medical devices, or other regulated industries. Interns typically work remotely, assisting with regulatory submissions, researching guidelines, and ensuring compliance with government regulations. This role helps develop essential skills in regulatory strategy, documentation, and communication while providing exposure to industry standards and processes.

What are the key skills and qualifications needed to thrive in the Remote Regulatory Affairs Internship position, and why are they important?

To thrive as a Remote Regulatory Affairs Intern, you should have a strong educational background in life sciences or a related field, sharp attention to detail, and solid research and writing skills. Familiarity with regulatory databases, document management software, and basic knowledge of FDA, EMA, or other regulatory authority guidelines is often required. Strong organizational skills, proactive communication, and the ability to work independently are key soft skills in a remote setting. These competencies are essential for ensuring regulatory compliance, timely document preparation, and effective collaboration within dispersed teams.

What types of projects or responsibilities can I expect as a Remote Regulatory Affairs Intern?

As a Remote Regulatory Affairs Intern, you will typically assist with preparing and reviewing regulatory documents, conducting research on regulatory requirements, and helping to track compliance deadlines. You may be involved in maintaining regulatory databases, supporting the team in submissions to health authorities, and organizing essential documents for audits or inspections. Collaboration is often conducted through virtual meetings, so clear and concise communication is key. This hands-on experience builds a solid foundation for a future career in regulatory affairs by exposing you to the processes and standards that govern product approvals.

What job categories do people searching Remote Regulatory Affairs Internship jobs in Decatur, GA look for? The top searched job categories for Remote Regulatory Affairs Internship jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Remote Regulatory Affairs Internship jobs? Cities near Decatur, GA with the most Remote Regulatory Affairs Internship job openings:
Remote Regulatory Affairs Internship jobs near you
Infographic showing various Remote Regulatory Affairs Internship job openings in Decatur, GA as of June 2026, with employment types broken down into 75% Full Time, 19% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $70,257 per year, or $33.8 per hour.

Remote Regulatory Affairs contractor

Globalchannelmanagement

Atlanta, GA • Remote

$99 - $100/hr

Full-time

Posted 2 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