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Remote Regulatory Submission Publisher Jobs in Riverside, NJ

micro1 AI

Director of Biostatistics

Philadelphia, PA · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Biostatistician

Philadelphia, PA · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Regulatory Affairs Specialist

Philadelphia, PA · Remote

$50 - $70/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... clinical submissions. * Documented experience drafting or leading responses to health authority ...

Exegenesis Bio Inc

Head of Regulatory Affairs

Ambler, PA · Remote

$153K - $202K/yr

Remote, US Exempt/Non-Exempt: Exempt Direct Reports : Yes Department: Regulatory Science EEO Job ... of successful submissions and license approvals with CDER and CBER * Extensive knowledge of ...

Exegenesis Bio Inc

Head of Regulatory Affairs

Ambler, PA · Remote

$153K - $202K/yr

Remote, US Exempt/Non-Exempt: Exempt Direct Reports : Yes Department: Regulatory Science EEO Job ... of successful submissions and license approvals with CDER and CBER * Extensive knowledge of ...

micro1 AI

Compliance Officers

Philadelphia, PA · Remote

$50 - $70/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... clinical submissions. * Documented experience drafting or leading responses to health authority ...

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Remote Regulatory Submission Publisher information

See Riverside, NJ salary details

$29

$57

$87

How much do remote regulatory submission publisher jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for remote regulatory submission publisher in Riverside, NJ is $57.54, according to ZipRecruiter salary data. Most workers in this role earn between $42.50 and $67.26 per hour, depending on experience, location, and employer.

What is a remote regulatory submission publisher?

A Remote Regulatory Submission Publisher is a professional who prepares, formats, and submits regulatory documents to health authorities, such as the FDA or EMA, from a remote location. Their primary responsibility is to ensure that all regulatory submissions comply with current guidelines and technical requirements. They use specialized software to compile, validate, and publish documents, often as part of the drug development process in the pharmaceutical or biotech industries. Working remotely allows them to perform these tasks from anywhere, collaborating virtually with regulatory and project teams.

What are the key skills and qualifications needed to thrive as a remote regulatory submission publisher?

To thrive as a Remote Regulatory Submission Publisher, you need expertise in regulatory submission processes, document management, and a background in life sciences or a related field. Familiarity with eCTD publishing tools (like Lorenz or Veeva Vault), regulatory databases, and understanding of global submission requirements is typically expected. Attention to detail, strong organizational skills, and effective remote communication are crucial soft skills for coordinating with cross-functional teams. These competencies ensure accurate, compliant, and timely submissions to regulatory authorities, which is critical for product approvals and company success.

What are some typical challenges faced by remote regulatory submission publishers, and how can they be effectively managed?

Remote Regulatory Submission Publishers often encounter challenges such as coordinating across multiple time zones, ensuring timely document collection from diverse teams, and maintaining compliance with varying global regulatory requirements. Effective management involves establishing clear communication channels, using collaborative document management systems, and staying updated on submission guidelines for different regions. Proactive organization and regular check-ins with cross-functional teams can help overcome these challenges, ensuring high-quality and compliant submissions.

What is the difference between Remote Regulatory Submission Publisher vs Remote Regulatory Affairs Associate?

AspectRemote Regulatory Submission PublisherRemote Regulatory Affairs Associate
CredentialsTypically requires a degree in life sciences or related field, with experience in document managementRequires a degree in life sciences, with knowledge of regulatory processes and possibly certification in regulatory affairs
Work EnvironmentPrimarily focused on preparing, formatting, and submitting regulatory documentsInvolves broader regulatory strategy, communication with authorities, and compliance oversight
Industry UsageCommonly employed in pharmaceutical, biotech, and medical device industries for submission tasksUsed across similar industries, with additional responsibilities in regulatory planning and strategy

The Remote Regulatory Submission Publisher mainly handles the preparation and submission of regulatory documents, focusing on formatting and compliance. In contrast, the Remote Regulatory Affairs Associate has a broader role, including regulatory strategy, communication, and compliance oversight. Both roles require relevant life sciences credentials but differ in scope and responsibilities.

What cities near Riverside, NJ are hiring for Remote Regulatory Submission Publisher jobs?

Cities near Riverside, NJ with the most Remote Regulatory Submission Publisher job openings:

Remote Regulatory Submission Publisher jobs near you
Infographic showing various Remote Regulatory Submission Publisher job openings in Riverside, NJ as of August 2026, with employment types broken down into 78% Full Time, 12% Part Time, 2% Temporary, and 8% Contract. Highlights an 100% Remote job distribution, with an average salary of $119,677 per year, or $57.5 per hour.

Regulatory Affairs Expert - Remote

YO AI Labs

Philadelphia, PA • Remote

$50 - $80/hr

Full-time

Posted 13 days ago

Job description

Job Title: Regulatory Affairs Specialist
Location: Remote
Job Type: ContractJob Description

We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating regulatory documentation. The role involves assessing clinical documents, ensuring compliance with regulatory guidelines, identifying inconsistencies, and providing clear, evidence-based feedback to improve AI-generated regulatory content.

Key Responsibilities

  • Review and evaluate clinical and regulatory documentation.

  • Assess regulatory submissions and responses for accuracy and compliance.

  • Ensure adherence to ICH guidelines and CTD/eCTD requirements.

  • Identify regulatory risks, inconsistencies, and unsupported claims.

  • Prepare structured, guideline-based written feedback.

Required Qualifications

  • 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry.

  • Experience with clinical submissions, regulatory documentation, and health authority interactions.

  • Strong knowledge of ICH guidelines and CTD/eCTD structure.

  • Excellent analytical, critical thinking, and written communication skills.

  • Degree in Life Sciences, Pharmacy, Medicine, or a related field.