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Regulatory Fda Remote Jobs (NOW HIRING)

Mercor

Regulatory Counsel

New York, NY · Remote

$85 - $120/hr

Remote Commitment: 20-40 hours/week Role Responsibilities * Design realistic regulatory scenarios ... Familiarity with regulatory portals like FDA , federalregister.gov , NLRB.gov , EEOC . Start Date

RadNet

Sr Regulatory Affair Principal

Somerville, MA · On-site +1

Lead and manage regulatory submissions, including FDA Q-submission, US 510(k)s submissions ... Working Environment Remote. This position requires domestic / international travel up to 15%

RadNet

Sr Regulatory Affair Principal

Somerville, MA · Remote

$130K - $160K/yr

Lead and manage regulatory submissions, including FDA Q-submission, US 510(k)s submissions ... Working Environment Remote. This position requires domestic / international travel up to 15%

Exegenesis Bio Inc

Head of Regulatory Affairs

Ambler, PA · Remote

$153.50K - $202.70K/yr

Remote, US Exempt/Non-Exempt: Exempt Direct Reports : Yes Department: Regulatory Science EEO Job ... Provide counsel, training and interpretation of FDA and other regulatory issues to company ...

Exegenesis Bio Inc

Head of Regulatory Affairs

Ambler, PA · Remote

$153.50K - $202.70K/yr

Remote, US Exempt/Non-Exempt: Exempt Direct Reports : Yes Department: Regulatory Science EEO Job ... Provide counsel, training and interpretation of FDA and other regulatory issues to company ...

RPM ReSearch

Head of Regulatory Affairs (Boston)

Boston, MA · Remote

$163.40K - $215.80K/yr

This fully remote role (US or Canada) will lead regulatory strategy, execution, and compliance ... Ensure compliance with FDA and Health Canada requirements, including CTA and IND processes.

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How much do regulatory fda remote jobs pay per hour?

As of May 30, 2026, the average hourly pay for regulatory fda remote in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Regulatory Affairs Specialist (FDA Remote), and why are they important?

To thrive as a Regulatory Affairs Specialist (FDA Remote), you need a solid understanding of FDA regulations, submission processes, and typically a degree in life sciences or a related field. Familiarity with regulatory submission tools such as eCTD, regulatory databases, and document management systems is essential. Strong attention to detail, effective written communication, and organizational skills help professionals excel in remote, deadline-driven environments. These skills ensure accurate and timely regulatory filings, compliance with changing guidelines, and effective collaboration with internal and external stakeholders.

How does working remotely in a Regulatory FDA role impact collaboration with cross-functional teams?

Remote Regulatory FDA professionals frequently collaborate with colleagues in clinical, legal, quality, and scientific departments through virtual meetings, shared platforms, and cloud-based document management systems. To remain effective, strong communication skills and proactive scheduling are essential, as regulatory deadlines often require swift, coordinated responses. While being remote allows flexibility, it can also present challenges in staying updated with rapidly changing regulations and ensuring alignment with team objectives. Regular check-ins and clear documentation help maintain workflow efficiency and compliance.

What does a Regulatory FDA Remote professional do?

A Regulatory FDA Remote professional is responsible for ensuring that a company’s products—such as pharmaceuticals, medical devices, or food items—comply with all U.S. Food and Drug Administration (FDA) regulations and guidelines. Working remotely, they prepare and submit regulatory documents, communicate with regulatory agencies, and interpret FDA requirements for their organization. Their work helps companies achieve and maintain approval for their products while minimizing regulatory risks. This role often involves collaborating with product development, quality assurance, and legal teams to ensure ongoing compliance.

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

AspectRegulatory Fda RemoteRegulatory Affairs Specialist
CertificationsFDA-related certifications, such as CDRH or CDRH-specific trainingRegulatory affairs certifications, like RAC or RAPS
Work EnvironmentPrimarily remote, focusing on FDA compliance documentation and submissionsOften office-based or hybrid, involved in broader regulatory strategies
Industry UsageCommon in medical device, pharmaceutical, and biotech companiesUsed across healthcare, medical devices, and pharmaceutical sectors

While both roles involve regulatory compliance, Regulatory Fda Remote positions focus specifically on FDA submissions and documentation remotely, whereas Regulatory Affairs Specialists handle broader regulatory strategies and may work onsite or hybrid. The roles often overlap in certifications and industry applications, but their scope and work environment differ.

More about Regulatory Fda Remote jobs
What cities are hiring for Regulatory Fda Remote jobs? Cities with the most Regulatory Fda Remote job openings:
What states have the most Regulatory Fda Remote jobs? States with the most job openings for Regulatory Fda Remote jobs include:
What job categories do people searching Regulatory Fda Remote jobs look for? The top searched job categories for Regulatory Fda Remote jobs are:
Regulatory Fda Remote jobs near you
Infographic showing various Regulatory Fda Remote job openings in the United States as of May 2026, with employment types broken down into 85% Full Time, 10% Part Time, and 5% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Regulatory Counsel

Mercor

New York, NY • Remote

$85 - $120/hr

Full-time

Posted 10 days ago

Job description

About the job

Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey.

Position: Legal Expert — Compliance / Regulatory (Remote, Hourly)
Type: Contract
Compensation: $85–$120/hour
Location: Remote
Commitment: 20–40 hours/week

Role Responsibilities

  • Design realistic regulatory scenarios from your practice, such as AML/SAR preparation, OFAC screening, and FCPA assessments.
  • Write "golden" reference responses at attorney-level quality.
  • Grade AI-generated responses against structured rubrics.
  • Provide written feedback to the research team to improve model behavior.
  • Participate in onboarding office hours and specialty calibration sessions.

Qualifications

Must-Have

  • 1–4 years of professional experience in regulatory or compliance law.
  • Hold a J.D. (U.S./Canada) or LL.B./LL.M. (U.K.) from an accredited law school.
  • Licensed to practice law in the U.S., Canada, or U.K. (active or inactive).
  • Strong experience with AML/BSA, OFAC sanctions screening, FCPA/anti-corruption, or healthcare regulatory.
  • Excellent written communication skills with high attention to detail.

Preferred

  • CIPP, CFE, CAMS, or similar certification.
  • Internal compliance investigation experience.
  • Experience drafting compliance training programs.
  • Familiarity with regulatory portals like FDA, federalregister.gov, NLRB.gov, EEOC.

Start Date

  • Immediately; applications reviewed on a rolling basis.

Compensation & Legal

  • Hourly contractor, Paid weekly via Stripe Connect.

Application Process (Takes 20–30 mins to complete)

  • Upload resume
  • AI interview based on your resume
  • Submit form

Resources & Support

  • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome
  • For any help or support, reach out to: support@mercor.com

PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.