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Regulatory Project Jobs (NOW HIRING)

IQVIA

Regulatory Project Manager

Durham, NC · On-site

$97K - $270K/yr

... regulatory strategy and execution across development stages, including major submissions, global registration activities, and, where applicable, post-marketing activities. Strong project and program ...

Nutanix

$134K - $162K/yr

The Manager, Regulatory Project Management is responsible for planning, executing, and driving regulatory submissions and regulatory project activities across clinical and nonclinical programs. This ...

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Regulatory Project information

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How much do regulatory project jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for regulatory project in the United States is $53.12, according to ZipRecruiter salary data. Most workers in this role earn between $37.98 and $68.99 per hour, depending on experience, location, and employer.

What is a regulatory project manager?

A Regulatory Project Manager is a professional who oversees and coordinates regulatory activities for organizations, particularly in industries like pharmaceuticals, biotechnology, and medical devices. Their primary responsibility is to ensure that products comply with all relevant regulations and standards, managing submissions to regulatory authorities and tracking progress through the approval process. They collaborate with cross-functional teams, develop regulatory strategies, and keep up-to-date with changing regulations to ensure successful product launches. Effective Regulatory Project Managers possess strong project management, communication, and analytical skills.

What are the key skills and qualifications needed to thrive as a regulatory project manager?

To thrive as a Regulatory Project Manager, you need a solid understanding of regulatory requirements, project management principles, and industry standards, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, project management tools like MS Project, and certifications such as PMP or RAC are highly valued. Strong organizational, communication, and problem-solving skills help manage cross-functional teams and adapt to evolving regulations. These skills ensure timely regulatory submissions, compliance, and effective coordination throughout complex projects.

How does a regulatory project manager typically collaborate with cross-functional teams during the product development lifecycle?

A Regulatory Project Manager works closely with teams such as R&D, Quality Assurance, Clinical, and Marketing to ensure that all regulatory requirements are met throughout the product development process. They facilitate communication between departments, coordinate the preparation and submission of regulatory documents, and help troubleshoot compliance issues as they arise. This role requires effective project management and strong interpersonal skills to align team efforts with regulatory timelines and standards, ensuring a smooth path to product approval.

What is the difference between Regulatory Project vs Regulatory Affairs Specialist?

AspectRegulatory ProjectRegulatory Affairs Specialist
CertificationsOften requires project management and regulatory certificationsTypically holds certifications like RAC or RA
Work EnvironmentFocuses on managing specific regulatory projects within teamsHandles ongoing regulatory compliance and submissions
Employer & Industry UsageCommon in pharmaceutical, biotech, and medical device companiesWidely used across similar industries for compliance roles

While both roles operate within regulatory frameworks, Regulatory Project managers oversee specific projects ensuring timely compliance, whereas Regulatory Affairs Specialists handle continuous regulatory activities and submissions. The roles often collaborate but differ in scope and focus.

What cities are hiring for Regulatory Project jobs?

Cities with the most Regulatory Project job openings:

What are the most commonly searched types of Regulatory Project jobs?

The most popular types of Regulatory Project jobs are:

What states have the most Regulatory Project jobs?

States with the most job openings for Regulatory Project jobs include:

What are popular job titles related to Regulatory Project jobs?

For Regulatory Project jobs, the most frequently searched job titles are:

Regulatory Project jobs near you
Infographic showing various Regulatory Project job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $110,486 per year, or $53.1 per hour.

Regulatory Project Manager

Durham, NC • On-site

IQVIA
Health Care and Social Assistance • 10K+ employees
Learn more about IQVIAexternal

$97K - $270K/yr

Full-time

Posted 8 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

Job description

The individual will support one or more global development programs as part of our Global Regulatory Science organization. The specific therapeutic area and program assignment will be determined based on the candidate's experience, capabilities, and fit with the team. This individual will support across both early- and late-stage development programs.
The role will partner closely with Global Regulatory Leads and cross-functional stakeholders to translate regulatory strategy into integrated, executable plans; manage key milestones, timelines, dependencies, risks, and regulatory deliverables; and help drive alignment and accountability across global regulatory teams. The individual will also support effective Global Regulatory Subteam governance, including meeting planning and facilitation, decision and action tracking, stakeholder communication, and follow-through on key regulatory activities.
Candidates with strong experience supporting global regulatory development programs, with particular emphasis on the US, EU, Canada, Australia, and UK. Exposure to APAC and LATAM markets is desirable, although deep regional expertise in those geographies is not required.
Ideal candidates will have:
Significant pharmaceutical or biotechnology experience, including substantial experience in regulatory affairs and/or regulatory program management.
Experience supporting regulatory strategy and execution across development stages, including major submissions, global registration activities, and, where applicable, post-marketing activities.
Strong project and program management capabilities, including management of complex timelines, interdependencies, risks, and cross-functional deliverables.
Demonstrated ability to work effectively in a matrixed global organization and partner with senior regulatory and cross-functional stakeholders.
Strong communication, facilitation, organizational, and influencing skills.
Familiarity with regulatory systems and tools; experience with Smartsheet, Microsoft Office/PPT-based timeline visualization tools, and Veeva RIM would be beneficial.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $97,200.00 - $270,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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