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Remote Regulatory Submission Publisher Jobs in Raleigh, NC

Recruit Up, LLC

Regulatory Writer

Chapel Hill, NC · Remote

... submissions for pharmaceutical, biotech, and medical device organizations ... Since 2006, they have supported global clients with a fully remote team of scientifically trained ...

New

Recruit Up, LLC

Regulatory Writer

Chapel Hill, NC · Remote

... submissions for pharmaceutical, biotech, and medical device organizations ... Since 2006, they have supported global clients with a fully remote team of scientifically trained ...

New

ViiV Healthcare

Principal Medical Writer

Durham, NC · Remote

Experience leading regulatory submission projects, including Common Technical Document (CTD ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · Remote

Experience leading regulatory submission projects, including Common Technical Document (CTD ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

Remote Schedule: Full-Time | Eastern Time Zone Hours Pay: $62.00-$64.73 per hour Position Overview ... Coordinate study start-up activities and support timely ethics committee and regulatory submissions.

princeps technologies

Clinical Data Manager

Raleigh, NC · On-site +1

United States or Canada (Remote/Hybrid) Employment Type : Full-Time Position Overview We are ... regulatory submissions Required Qualifications Bachelor's degree in Life Sciences, Pharmacy, or a ...

New

princeps technologies

Clinical Data Manager

Raleigh, NC · On-site +1

United States or Canada (Remote/Hybrid) Employment Type : Full-Time Position Overview We are ... regulatory submissions Required Qualifications Bachelor's degree in Life Sciences, Pharmacy, or a ...

New

Danaher

Principal Clinical Scientist

Raleigh, NC · On-site +1

... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...

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Remote Regulatory Submission Publisher information

See Raleigh, NC salary details

$28

$55

$84

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

As of Aug 31, 2026, the average hourly pay for remote regulatory submission publisher in Raleigh, NC is $55.38, according to ZipRecruiter salary data. Most workers in this role earn between $40.91 and $64.71 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 are the most commonly searched types of Regulatory Submission Publisher jobs in Raleigh, NC?

The most popular types of Regulatory Submission Publisher jobs in Raleigh, NC are:

What are popular job titles related to Remote Regulatory Submission Publisher jobs in Raleigh, NC?

For Remote Regulatory Submission Publisher jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Regulatory Submission Publisher jobs in Raleigh, NC look for?

The top searched job categories for Remote Regulatory Submission Publisher jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Regulatory Submission Publisher jobs?

Cities near Raleigh, NC 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 Raleigh, NC as of August 2026, with employment types broken down into 93% Full Time, 3% Temporary, and 4% Contract. Highlights an 100% Remote job distribution, with an average salary of $115,184 per year, or $55.4 per hour.

Regulatory Writer

Chapel Hill, NC • Remote

Recruit Up, LLC
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Recruit Up, LLCexternal

Full-time

Posted 2 days ago

New

Job description

Regulatory Writer Opportunity

Our client, located in Chapel Hill, NC, is a professional services company operating in a highly regulated space, specializing in medical writing, quality control review, and electronic regulatory submissions for pharmaceutical, biotech, and medical device organizations. Since 2006, they have supported global clients with a fully remote team of scientifically trained professionals across the U.S. The organization is known for innovation, having expanded its eCTD publishing capabilities and developed proprietary tools to enhance regulatory communication. As a woman-owned business, they are committed to excellence, integrity, and strong environmental and community stewardship.

They are currently seeking a Regulatory Writer to develop compliant medical documents, perform quality reviews, and prepare electronic submissions to support regulatory approvals using accurate scientific and clinical data.

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