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Remote Regulatory Advertising Promotion Jobs (NOW HIRING)

Advita Ortho

Sr Manager, Regulatory Affairs

US (Remote) Reporting To: Sr. Global Regulatory Affairs Director Description The Sr Manager ... Oversee the regulatory review and approval of post-launch advertising and promotion (A&P ...

New

Axiom Talent Platform

Marketing & Advertising Lawyer

OR · On-site +1

$309K/yr

Remote We are currently seeking Marketing & Advertising Lawyers to work with some of the world ... Experience reviewing website content, online campaigns, promotions, sweepstakes, and press releases ...

Scale Inc

Regulatory Affairs Specialist

Burbank, CA · Remote

Review and approve promotional materials -- commercial scripts, social media content, email, and ... Apply structure/function and advertising requirements to flag risky language and recommend ...

Exactech

Sr Manager, Regulatory Affairs

Oversee the regulatory review and approval of post-launch advertising and promotion (A&P); implement and maintain processes to ensure robust and timely pre-release review of A&P * Oversee compliance ...

New

Irhythmtech

Senior Regulatory Affairs Specialist

... a remote Senior Regulatory Affairs Specialist with a fast growing, AI software and wearable ... Review and approve advertising and promotional items to drive global labeling alignment as well as ...

New

iRhythm Holdings, Inc.

Manager, Regulatory Affairs

$127K - $165K/yr

Key Regulatory SME and review & approve advertising and promotional materials to ensure regulatory ... Remote - US Actual compensation may vary depending on job-related factors including knowledge ...

Irhythmtech

Manager, Regulatory Affairs

$127K - $165K/yr

Key Regulatory SME and review & approve advertising and promotional materials to ensure regulatory ... Remote - US Actual compensation may vary depending on job-related factors including knowledge ...

Irhythmtech

Manager, Regulatory Affairs

San Francisco, CA · On-site +1

$127K - $165K/yr

Key Regulatory SME and review & approve advertising and promotional materials to ensure regulatory ... Remote - US Actual compensation may vary depending on job-related factors including knowledge ...

Zimmer, Inc.

Regulatory Affairs Manager

... promotion and advertising material for compliance with applicable regulations, and reviews of ... While this is a remote position, strong preference will be given to candidates located in or near ...

Zimmer, Inc.

Regulatory Affairs Manager

... promotion and advertising material for compliance with applicable regulations, and reviews of ... While this is a remote position, strong preference will be given to candidates located in or near ...

VB Spine

Sr. Staff Regulatory Affairs Specialist

Leesburg, VA · On-site +1

$135K - $145K/yr

Allendale, NJ, Leesburg, VA, or Remote Company: VB Spine Looking for a career where your work truly ... Ensure compliance with post-approval/clearance requirements, labeling, advertising, and promotional ...

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All JobsRegulatory Advertising Promotion JobsRemote Regulatory Advertising Promotion Jobs

Remote Regulatory Advertising Promotion information

See salary details

$40.5K

$95.4K

$138.5K

How much do remote regulatory advertising promotion jobs pay per year?

As of Aug 16, 2026, the average yearly pay for remote regulatory advertising promotion in the United States is $95,411.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $112,000.00 per year, depending on experience, location, and employer.

How does a Remote Regulatory Advertising Promotion specialist typically collaborate with cross-functional teams to ensure compliance?

A Remote Regulatory Advertising Promotion specialist often works closely with marketing, legal, and medical affairs teams to review and approve promotional materials. Collaboration usually happens through virtual meetings, shared document platforms, and workflow management tools to ensure that all advertising content meets current regulatory requirements. Effective communication and timely feedback are key, as the specialist must interpret complex regulations and provide guidance to non-regulatory colleagues. This role requires balancing regulatory compliance with business objectives, making teamwork and adaptability essential skills.

What are the key skills and qualifications needed to thrive as a Remote Regulatory Advertising Promotion specialist, and why are they important?

To thrive as a Remote Regulatory Advertising Promotion Specialist, you need a solid understanding of FDA regulations, advertising standards, and pharmaceutical or medical device industry guidelines, often supported by a degree in life sciences or a related field. Familiarity with submission systems like OPDP eCTD, document management platforms, and regulatory tracking tools is typically required. Strong attention to detail, clear written communication, and the ability to collaborate cross-functionally are crucial soft skills. These competencies ensure that promotional materials are compliant, minimize regulatory risks, and support successful product marketing in a remote environment.

What is a Remote Regulatory Advertising Promotion specialist?

A Remote Regulatory Advertising Promotion specialist is a professional who ensures that a company's advertising and promotional materials comply with regulatory standards, such as those set by the FDA or other governing bodies. They review marketing content for products, especially in industries like pharmaceuticals and medical devices, to make sure claims are truthful, not misleading, and properly substantiated. Working remotely, they collaborate with marketing, legal, and compliance teams to guide the development of promotional materials and help avoid legal or regulatory issues. Their role is crucial in protecting the company from regulatory penalties and maintaining public trust.

What is the difference between Remote Regulatory Advertising Promotion vs Remote Medical Affairs?

AspectRemote Regulatory Advertising PromotionRemote Medical Affairs
Required credentialsLife sciences, marketing, or regulatory certificationsMedical, scientific, or healthcare-related degrees and certifications
Work environmentCollaborative with marketing, legal, and regulatory teamsScientific communication with healthcare professionals and internal teams
Employer and industry usagePharmaceutical, biotech, and healthcare industriesPharmaceutical and biotech sectors, focusing on scientific exchange
Common search and comparison intentUnderstanding roles in pharmaceutical marketing and complianceClarifying scientific communication and medical strategy roles

Remote Regulatory Advertising Promotion focuses on ensuring marketing materials comply with regulations and promoting products within legal boundaries. Remote Medical Affairs involves scientific communication, medical strategy, and supporting healthcare professionals. While both roles operate in the pharmaceutical industry, they serve different functions—one emphasizes compliance and promotion, the other scientific exchange and medical support.

More about Remote Regulatory Advertising Promotion jobs

What cities are hiring for Remote Regulatory Advertising Promotion jobs?

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What are the most commonly searched types of Regulatory Advertising Promotion jobs?

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States with the most job openings for Remote Regulatory Advertising Promotion jobs include:

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The top searched job categories for Remote Regulatory Advertising Promotion jobs are:

Remote Regulatory Advertising Promotion jobs near you
Infographic showing various Remote Regulatory Advertising Promotion job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, 20% Part Time, and 30% Contract. Highlights an 10% In-person, and 90% Remote job distribution, with an average salary of $95,411 per year, or $45.9 per hour.

Sr Manager, Regulatory Affairs

Advita Ortho

Remote

Full-time

Posted 2 days ago

New

Job description

Sr Manager, Regulatory Affairs
Department: Regulatory
Employment Type: Full Time
Location: US (Remote)
Reporting To: Sr. Global Regulatory Affairs Director
Description
The Sr Manager, Regulatory Affairs provides strategic leadership for and oversight of the Lifecycle (Postmarket) Regulatory team accountable for Advita's postmarket regulatory affairs, i.e., regulatory support of commercialized products. Accountabilities include activities such as assessment of proposed changes for regulatory impact, regulatory strategy and support for change projects, compliance with Conditions of Approval, EU renewals and regulatory review & approval of advertising and promotion. The Sr Manager, Regulatory Affairs will partner with the business (e.g., BUs, Operations, etc.) and regulatory colleagues (e.g., the BU, Regional and RO & RCoE RA teams) to develop and execute global regulatory strategies in support of commercialized products.
Key Responsibilities
  • Oversee the regulatory professionals who manage Advita's Lifecycle (postmarket) RA: recruit, hire, train, develop and direct the work activity of LC RA personnel
  • Communicate directly (also through LC RA team members) with regulatory agencies and health authorities regarding registrations, submissions and regulatory strategies
  • In partnership with the business and regulatory colleagues (e.g., BU, Operations, and the BU, Regional and RO & RCoE RA teams) develop and execute regulatory strategies and timelines to support proposed changes to commercialized product. Identify and communicate regulatory impact, regulatory requirements and submission deliverables, and execute to achieve regulatory milestones.
  • Provide input to the change teams on project and test plans, ensuring that the plans address all elements of the project regulatory strategy
  • Maintain awareness of the global regulatory environment; assess and communicate the impact of key environmental changes LC RA initiatives and strategies
  • Collaborate with trade associations and regulators to help shape the regulatory environment
  • Oversee the regulatory review and approval of post-launch advertising and promotion (A&P); implement and maintain processes to ensure robust and timely pre-release review of A&P
  • Oversee compliance with any regulatory Conditions of Approval; implement and maintain systems and/or processes to ensure conditions are met on time
  • Support regulatory audits and inspections Interpret and apply medical device regulations and standards

Skills Knowledge and Expertise
Education:
  • A minimum of a Bachelor's Degree from an accredited institution, preferably in physical or life sciences; Master's Degree preferred

Experience:
  • Minimum 10 years' experience in medical device industry in regulatory affairs or related field, orthopaedic device industry experience preferred.
  • Experience in US, EU and/or international submissions/registrations required
  • Working knowledge of US, EU and international medical device regulations required
  • Demonstrated experience leading in-depth technical and strategic discussions with Health Authorities required
  • Demonstrated ability to influence and negotiate with cross-functional partners and stakeholders, both internal and external required
  • Prior team leadership required
  • Regulatory Affairs Certification (RAC) preferred

Functional/Technical Knowledge, Skills and Abilities Required:
  • Proficiency with windows-based office productivity tools (Microsoft Office)

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