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Regulatory Project Manager Jobs (NOW HIRING)

ICON

Senior Regulatory Project Manager

Blue Bell, PA · On-site +1

Senior Regulatory Project Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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Senior Regulatory Project Manager

Reading, PA · On-site

Senior Regulatory Project Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

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Regulatory Project Manager information

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$38.5K

$102.7K

$162K

How much do regulatory project manager jobs pay per year?

As of Aug 20, 2026, the average yearly pay for regulatory project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

What is a regulatory project manager?

A Regulatory Project Manager is a professional responsible for overseeing and coordinating regulatory submissions and compliance activities within industries such as pharmaceuticals, biotechnology, or medical devices. They ensure that products meet all regulatory requirements throughout the development and approval process, working closely with cross-functional teams to prepare documentation for submission to regulatory agencies like the FDA or EMA. Their role involves project planning, timeline management, risk assessment, and communication with regulatory authorities to facilitate timely product approvals.

How does a regulatory project manager typically coordinate with cross-functional teams during a product submission process?

A Regulatory Project Manager plays a central role in coordinating cross-functional teams, such as R&D, clinical, quality assurance, and manufacturing, during product submission. They facilitate regular meetings, ensure all stakeholders are aligned on timelines and regulatory requirements, and manage documentation flow to meet submission deadlines. Effective communication and proactive issue resolution are key to successfully navigating the complex regulatory landscape and ensuring projects stay on track. This collaborative approach not only streamlines the submission process but also helps anticipate and mitigate potential regulatory challenges.

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

To thrive as a Regulatory Project Manager, you need a solid understanding of regulatory affairs, project management principles, and often a relevant degree in life sciences or a related field. Familiarity with project management software, regulatory submission platforms, and certifications such as PMP or RAC are highly valued. Strong organizational, leadership, and communication skills set top performers apart in this role. These competencies are crucial for ensuring regulatory compliance, timely project delivery, and effective coordination between cross-functional teams.

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

AspectRegulatory Project ManagerRegulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences, engineering, or related field; certifications like RAC are commonSimilar credentials; often holds a degree in life sciences and RAC certification
Work EnvironmentManages projects across teams, coordinates regulatory submissions, and ensures compliance timelinesFocuses on preparing regulatory documents, liaising with authorities, and maintaining compliance documentation
Employer & Industry UsageUsed in pharmaceutical, biotech, and medical device companies for project oversightCommon in regulatory departments within similar industries for document preparation and submission

While both roles require regulatory knowledge and similar credentials, the Regulatory Project Manager primarily oversees regulatory projects and timelines, whereas the Regulatory Affairs Specialist concentrates on preparing and managing regulatory submissions and documentation.

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Regulatory Project Manager jobs near you
Infographic showing various Regulatory 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 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Global Regulatory Project Manager

Corteva, Inc.

Indianapolis, IN • On-site

Full-time

Medical, Retirement, PTO

Posted 17 days ago

Corteva Agriscience rating

8.3

Company rating: 8.3 out of 10

Based on 75 frontline employees who took The Breakroom Quiz

48th of 542 rated manufacturers

Job description

Who are we, and what do we do?
At Corteva Agriscience, you will help us grow what's next. No matter what your role, you will be part of a team that is building the future of agriculture - solving the world's food problems through innovation, technology, and putting people first.
Corteva Agriscience is seeking an experienced Global Regulatory Project Manager (GRPM) to join our dynamic team
This Global Regulatory Project Manager (GRPM) sits within a global regulatory organization responsible for enabling product registrations across a broad range of technologies and markets, supporting business growth through effective regulatory execution.
Purpose
The Global Regulatory Project Manager (GRPM) translates regulatory strategy and plans into actionable execution by developing implementation plans, key milestones, and budget oversight. The role holds end-to-end accountability for managing regulatory plans from initiation through completion, proactively identifying and managing risks to the critical path.
The GRPM serves as the overall project manager for a portfolio of regulatory projects, enabling timely submissions and sustained market access through disciplined execution within a matrix organization.
Key Interactions
The GRPM works in close partnership with regulatory affairs and regulatory sciences teams to ensure joint accountability across regulatory, scientific, and project management dimensions.
The role collaborates extensively with global, regional, and country stakeholders, including subject matter experts, regulatory science leaders, business partners, and regional and country regulatory leaders to align priorities, execution, and outcomes.
Key Responsibilities
Program & Portfolio Leadership
  • Provide project and program leadership across products at different R&D stages and lifecycle phases within assigned regulatory portfolios.
  • Translate regulatory and business strategy into executable plans, timelines, milestones, and priorities.
  • Monitor the critical path, proactively identifying vulnerabilities, risks, or delays, and engaging stakeholders to address them.

Study Execution, Submissions & Market Access
  • Coordinate the planning and execution of regulatory studies in collaboration with regulatory stakeholders.
  • Integrate study delivery, dependencies, and outcomes into overall regulatory plans to enable on-time submissions and market access.

Governance, Risk & Change Management
  • Facilitate effective governance and decision-making by enabling structured discussions, prioritization, and trade-off assessments.
  • Proactively manage risks, changes, and dependencies that may impact regulatory timelines or outcomes.
  • Act as a change agent, driving adoption of consistent ways of working across teams.

Team Alignment & Collaboration
  • Facilitate global regulatory team interactions to ensure alignment, decision clarity, and follow-through.
  • Maintain close connection with regional and country teams to support submission planning and execution.
  • Share learnings and best practices across the broader regulatory organization.

Competencies & Leadership Expectations
  • Execution leadership and accountability in complex, matrixed environments
  • Strong stakeholder influence without direct authority
  • Sound judgment and problem-solving in ambiguous situations
  • Governance mindset combined with openness to change
  • High learning agility and adaptability to evolving tools, processes, and operating models

Capabilities & Experience
  • Proven experience leading complex initiatives within global, matrixed organizations.
  • Demonstrated ability to coordinate study execution in support of regulatory submissions and approvals.
  • Experience operating within governance frameworks and cross-functional decision forums.
  • Ability to operate effectively across regulatory jurisdictions, technical disciplines, and global time zones.
  • Strong ability to learn, adopt, and leverage project management and data/analytics solutions.

Required Qualifications
  • Bachelor's degree in a scientific, technical, business, or related field.
  • Experience in regulatory, scientific, or complex cross-functional project environments.
  • Strong facilitation, communication, and stakeholder management skills.

#LI-BB1
Benefits - How We'll Support You:
  • Numerous development opportunities offered to build your skills
  • Be part of a company with a higher purpose and contribute to making the world a better place
  • Health benefits for you and your family on your first day of employment
  • Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays
  • Excellent parental leave which includes a minimum of 16 weeks for mother and father
  • Future planning with our competitive retirement savings plan and tuition reimbursement program
  • Learn more about our total rewards package here - Corteva Benefits
  • Check out life at Corteva! www.linkedin.com/company/corteva/life

Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team.
Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.

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