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Remote Regulatory Submission Publisher Jobs in Boca Raton, FL

BidMachine

Lead In‑House Legal Counsel

Parkland, FL · Remote

... remote experts around the world. We combine deep AdTech expertise, proprietary technology, and a ... Our mission is to create a high-performance marketplace where publishers maximize value and ...

Sage Dental

Credentialing Specialist

Boca Raton, FL · On-site +1

In all activities, they must comply with all legal and regulatory policies and procedures ... Insurance/Payer Application submission experience * Designated workspace with high-speed internet ...

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All JobsRegulatory Submission Publisher JobsRemote Regulatory Submission Publisher JobsRemote Regulatory Submission Publisher Jobs in Boca Raton, FL

Remote Regulatory Submission Publisher information

See Boca Raton, FL salary details

$27

$54

$82

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

As of Sep 3, 2026, the average hourly pay for remote regulatory submission publisher in Boca Raton, FL is $54.06, according to ZipRecruiter salary data. Most workers in this role earn between $39.90 and $63.17 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 job categories do people searching Remote Regulatory Submission Publisher jobs in Boca Raton, FL look for?

The top searched job categories for Remote Regulatory Submission Publisher jobs in Boca Raton, FL are:

What cities near Boca Raton, FL are hiring for Remote Regulatory Submission Publisher jobs?

Cities near Boca Raton, FL 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 Boca Raton, FL as of August 2026, with employment types broken down into 81% Full Time, 7% Temporary, and 12% Contract. Highlights an 100% Remote job distribution, with an average salary of $112,445 per year, or $54.1 per hour.

Senior Manager Regulatory Affairs

Syncromune

Fort Lauderdale, FL • On-site, Remote

$160K - $180K/yr

Full-time

Posted 14 days ago

Job description

The Senior Manager of Regulatory Affairs will assist in all facets of the company's Regulatory Affairs for all U.S. and international regulatory matters, including filings and interactions with regulatory authorities.
Principal Duties and Responsibilities include the following:
The following is not intended to be an all-inclusive list of responsibilities. Other activities may be assigned as required by management.
  • Support the Senior Director of Regulatory Affairs to ensure adherence to appropriate regulations and standards.
  • Assists with determining regulatory requirements and prepare regulatory submission for all new/modified combination products, drugs, and medical devices. These submissions can include but not be limited to IND's, BLA's, meeting packages and expediated programs.
  • Provide strategic input on development plans and sequencing of regulatory submissions (participate in the coordination, preparation and timely submission of regulatory documents).
  • Anticipate and mitigate regulatory risks; proactively identify opportunities for regulatory flexibility, expedited programs, and innovative pathways.
  • Partner closely with cross-functional teams and influence program decision-making by integrating regulatory considerations early and consistently.
  • Ensure project teams prepare high quality international and domestic filings/registrations and responses to agency requests within established timelines.
  • Review submission packages for compliance with global regulations.
  • Write and edit technical documents.
  • Review and create standard operating procedures (SOPs).
  • Ensure regulatory documentation is maintained appropriately.
  • Interact with regulatory agencies as required.
  • Contribute to the evolution of regulatory strategy capabilities, regulatory internal processes, and best practices within the organization.
  • Promote a culture of scientific rigor, regulatory strategy excellence, and proactive risk evaluation.
Supervisory Responsibilities:
  • None
Qualification Requirements:
Education:
  • Bachelor's Degree in Life Sciences, Engineering or related field
  • Master's degree preferred
Experience:
  • 5+ years in a regulatory capacity at a pharmaceutical company, biotech or CRO with 2+ years supporting oncology products.
  • High degree of understanding of regulatory requirements, how they operate, how to obtain updated information and where to obtain interpretations of them
  • Experience in authoring part of regulatory documents such as M1, M2 of an IND, IND amendments, response to regulatory agency's IR, expediated program applications.
  • Ability to inform and educate managers and department heads on regulations and policies that require compliance
  • Ability to translate regulatory requirements into practical, workable plans
  • Proficient with Microsoft Office Suite or similar software
  • Proficient with applicable database and compliance software
  • Must be able to juggle multiple and competing priorities
Knowledge/Skill:
  • Excellent organizational and project management skills.
  • Ability to work on multiple projects simultaneously with flexibility to take on new challenges as needed.
  • Excellent attention to detail.
  • Must have outstanding communication and collaboration skills within cross-functional teams and external organizations.
  • Ability to work in a fast-paced virtual environment.
  • Excellent verbal and writing skills.
  • Excellent analytical and problem-solving skills
  • Excellent editing and proof-reading skills.
  • Possess a self-directing, self-starting work ethic.
  • Excellent knowledge of the competitive environment for drugs in the oncology marketplace and in research and development pipelines.
Working Conditions:
  • The work environment shall be split between a virtual office environment and the Company headquarters in Fort Lauderdale, FL.
  • Domestic travel up to 10% of time
  • Ability to lift up to 25 pounds
  • Regularly required to stand, sit, talk, hear, and use hands
  • Prolonged periods of sitting and standing
Syncromune is an Equal Opportunity Employer.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate's relevant skills, experience, and education.
Expected US salary range: $160,000-180,000
This position generally is eligible for cash incentive compensation, equity incentive compensation, and employee benefits under the Company's benefit plans.
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