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Regulatory Documentation Manager Jobs in Raleigh, NC

Regulatory Coordinator

Durham, NC · On-site

$61K - $101K/yr

Manage study-level regulatory documentation and compliance activities, including preparation for monitoring visits, audits, study closeout, and document storage. * Coordinate site visits and ...

Regulatory Coordinator

Durham, NC · On-site

$61K - $101K/yr

Manage study-level regulatory documentation and compliance activities, including preparation for monitoring visits, audits, study closeout, and document storage. * Coordinate site visits and ...

Regulatory Affairs Manager

Durham, NC · On-site

$90 - $120/hr

Regulatory Affairs Manager Bioventus is a global leader in developing clinically proven ... Prepare and oversee documentation packages for submission to global regulatory authorities to ...

The Regulatory Affairs Manager is responsible for developing and executing global regulatory ... Key Responsibilities: 1. Prepare, provide direction and oversee documentation packages for ...

The Regulatory Affairs Manager is responsible for developing and executing global regulatory ... Key Responsibilities: 1. Prepare, provide direction and oversee documentation packages for ...

The Regulatory Affairs Manager is responsible for developing and executing global regulatory ... Key Responsibilities: 1. Prepare, provide direction and oversee documentation packages for ...

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Showing results 1-20

Regulatory Documentation Manager information

See Raleigh, NC salary details

$53K

$107.6K

$176.9K

How much do regulatory documentation manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for regulatory documentation manager in Raleigh, NC is $107,641.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,300.00 and $132,700.00 per year, depending on experience, location, and employer.

What is the difference between Regulatory Documentation Manager vs Regulatory Affairs Specialist?

AspectRegulatory Documentation ManagerRegulatory Affairs Specialist
Primary FocusManaging and overseeing regulatory documentation processesEnsuring compliance and preparing regulatory submissions
Required CredentialsTypically a degree in life sciences or related field, with experience in documentationSimilar credentials, often with additional certification in regulatory affairs
Work EnvironmentRegulatory or compliance departments within pharmaceutical or medical device companiesRegulatory departments, often collaborating across teams
Industry UsageCommonly used in regulated industries like pharma and medical devicesWidely used in the same industries, often with overlapping responsibilities

While both roles operate within regulated industries and require knowledge of compliance standards, the Regulatory Documentation Manager primarily oversees the management of regulatory documents, whereas the Regulatory Affairs Specialist focuses on ensuring overall regulatory compliance and preparing submissions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are popular job titles related to Regulatory Documentation Manager jobs in Raleigh, NC?

For Regulatory Documentation Manager jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Regulatory Documentation Manager jobs in Raleigh, NC look for?

The top searched job categories for Regulatory Documentation Manager jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Regulatory Documentation Manager jobs?

Cities near Raleigh, NC with the most Regulatory Documentation Manager job openings:

Infographic showing various Regulatory Documentation Manager job openings in Raleigh, NC as of June 2026, with employment types broken down into 1% As Needed, 65% Full Time, 32% Part Time, 1% Temporary, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $107,641 per year, or $51.8 per hour.

Regulatory Affairs Specialist

Peregrine Team

Raleigh, NC • On-site

Full-time

Re-posted 2 days ago


Job description

Peregrine Team is seeking a Regulatory Affairs Specialist to support global regulatory submissions and ensure compliance across pharmaceutical products. This role will work closely with cross-functional teams to support product approvals and lifecycle management.
Key Responsibilities
  • Prepare and submit regulatory filings (IND, NDA, BLA, etc.)
  • Track and interpret regulatory requirements across global markets
  • Support product lifecycle management and labeling updates
  • Collaborate with QA, clinical, and manufacturing teams
  • Maintain regulatory documentation and databases

Qualifications
  • Bachelor's degree in Life Sciences or related field
  • 3-6+ years of regulatory experience in pharma/biotech
  • Knowledge of FDA and international regulatory guidelines
  • Strong writing and analytical skills

Peregrine Team logo

About Peregrine Team

Sourced by ZipRecruiter

Our Vision I started Peregrine Team with superior customer service and quality in mind. Going back to the basics. My team exists to challenge the lazy, idle and often sloppy recruiting and staffing teams out there. We see agency after agency spending less time with the people, not caring about what individuals are looking for when making a career move. Sourcing top talent is not easy in the current environment, but listening and caring about others will create trust, lasting partnerships and overall success. Whether you are looking for a job or looking for talent, we can help manage the process. We are a team of hunters, able to find and hire quality experienced professionals for any organization. We primarily specialize in placement of professionals in the Healthcare & Life Science space, but will take on any challenge. We simply do things differently.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Orange County, CA, US

Year founded

2021

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