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Regulatory Affairs Project Manager Jobs (NOW HIRING)

Medasource

Medical Affairs Project Manager

Horsham, PA · On-site

$75 - $80/hr

US Medical Affairs Project Manager (Solid Tumor- GU) Hybrid role; Horsham, PA ~1 day a week ... Ensure compliance with industry regulations and internal standards throughout project execution

FalconSmartIT

Medical Affairs Project Manager

San Mateo, CA · On-site

$140 - $180/hr

Understanding of compliance requirements within Medical Affairs organizations.8+ years of IT or Business Project Management experience.Proven track record managing enterprise application and business ...

New

Oterra

Regulatory Affairs Manager

Sturtevant, WI

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for ... Develop and implement regulatory strategies to support new product launches, innovation projects ...

New

Oterra

Regulatory Affairs Manager

Mount Pleasant, WI · On-site

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for ... Develop and implement regulatory strategies to support new product launches, innovation projects ...

Oterra

Regulatory Affairs Manager

Mount Pleasant, WI · On-site

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for ... Develop and implement regulatory strategies to support new product launches, innovation projects ...

Medasource

Medical Affairs Project Manager

Horsham, PA · On-site

$103.32 - $110.21/hr

US Medical Affairs Project Manager (Solid Tumor- GU) Hybrid role; Horsham, PA ~1 day a week ... Ensure compliance with industry regulations and internal standards throughout project execution

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How much do regulatory affairs project manager jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for regulatory affairs project manager in the United States is $56.97, according to ZipRecruiter salary data. Most workers in this role earn between $42.07 and $66.59 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a regulatory affairs project manager, and why are they important?

To thrive as a Regulatory Affairs Project Manager, you need a solid understanding of regulatory guidelines, project management principles, and a relevant science or engineering degree. Familiarity with regulatory submission systems (such as eCTD), project management tools (like MS Project), and certifications such as RAC are highly valued. Exceptional organizational, communication, and problem-solving abilities set top performers apart in this field. These skills ensure timely regulatory approvals, compliance with global standards, and effective coordination across cross-functional teams.

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

As a Regulatory Affairs Project Manager, you will regularly work with cross-functional teams such as R&D, quality assurance, clinical, and marketing to ensure that projects meet regulatory requirements at every stage. Your role involves coordinating timelines, communicating regulatory expectations, and integrating feedback to guide product development toward successful submissions. Effective collaboration is key, as you'll often lead meetings, resolve regulatory challenges, and provide expert advice to align the team's efforts with evolving global regulations.

What is a regulatory affairs project manager?

A Regulatory Affairs Project Manager is a professional who oversees and coordinates regulatory processes related to product development, approval, and compliance within industries such as pharmaceuticals, biotechnology, or medical devices. They ensure that products meet all required regulatory standards and are submitted to governmental agencies for approval on time. Their role involves managing timelines, collaborating with cross-functional teams, and staying up-to-date with changing regulations to minimize risks and facilitate product launches.

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

AspectRegulatory Affairs Project ManagerRegulatory Affairs Specialist
ResponsibilitiesOversees regulatory projects, manages teams, ensures compliance timelinesPrepares documentation, conducts research, supports regulatory submissions
Required CredentialsBachelor's degree, often with project management or regulatory certificationsBachelor's degree, regulatory affairs certifications beneficial
Work EnvironmentCross-functional teams, project-based settings, corporate officesRegulatory departments, laboratories, or manufacturing sites
Industry UsageCommon in pharmaceutical, biotech, medical device companiesWidely used in similar industries for compliance support

The Regulatory Affairs Project Manager focuses on leading regulatory projects, coordinating teams, and ensuring compliance deadlines are met. In contrast, the Regulatory Affairs Specialist handles detailed documentation, research, and supports submissions. Both roles require regulatory knowledge and certifications, but the Project Manager has a broader oversight role, often managing multiple projects simultaneously.

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Regulatory Affairs Project Manager jobs near you
Infographic showing various Regulatory Affairs Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $118,493 per year, or $57 per hour.

Senior Regulatory Affairs Consultant (Program / Client Partnership Manager)

Parexel

Remote

Full-time

Re-posted yesterday

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

29th of 73 rated research

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Due to continued growth and the ongoing success of our Regulatory Affairs Consulting team, Parexel is seeking an experienced Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) to join our team. In this pivotal role, you will leverage advanced Regulatory Affairs expertise alongside strong strategic and operational insight to deliver high-quality, tailored solutions for our clients. You will play a key leadership role in managing midsize to large Regulatory Affairs outsourcing programs, partnering closely with clients and cross-functional teams to drive operational excellence, ensure delivery against regulatory objectives, and support the successful progression of development and commercial programs.
As a trusted leader and client advisor, you will work with considerable autonomy, managing complex projects from inception to completion while mentoring the next generation of project leaders. This is an opportunity to make a significant impact on global Regulatory Affairs projects while contributing to business growth and client success.
Role Responsibilities:
Lead Client Solutions & Business Development
  • Act as a trusted advisor to clients on complex Regulatory Affairs challenges
  • Present Parexel's Regulatory Affairs Consulting capabilities and deliver customized sales presentations
  • Provide proposal support and oversight, participating in bid defense meetings
  • Generate new business through personal reputation and client relationships
  • Actively participate in strategic account planning for key clients

Drive Project Excellence
  • Provide cross-functional leadership for regulatory outsourcing programs and project teams
  • Deliver projects on time, within budget, and to the highest quality standards
  • Monitor profitability across multiple projects through active budget management
  • Proactively identify and resolve issues affecting project success and client satisfaction
  • Leverage best practices and industry knowledge to develop innovative business solutions

Mentorship & Develop Teams
  • Guide colleagues on appropriate project execution methods
  • Foster a collaborative team environment that drives results

Staying Ahead of Industry Trends
  • Monitor and evaluate industry initiatives, policy changes, and technology trends
  • Ensure delivery of cutting-edge solutions that meet evolving client needs
  • Maintain professional development and industry knowledge

Skills and Experience required for the role
  • Minimum of a Bachelor's Degree in a Scientific or Technical Discipline, Advanced Degree Preferred.
  • Extensive experience in life sciences or consulting industries with at least 5 years of experience in a related Program Management role
  • Proven track record managing Regulatory Affairs projects, client solutions, and teams
  • Demonstrated success in winning and leading global projects
  • Strong business development and proposal management experience
  • Advanced project management and operational leadership capabilities
  • Excellent consulting skills with a client-focused approach
  • Critical thinking and problem-solving abilities
  • Proven ability to influence, network, and hold people accountable
  • Budget management and financial forecasting expertise
  • Fluent English, written and spoken

#LI-LB1
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

What Parexel employees say

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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