Regulatory Strategy Consultant

I contribute to clinical research with expertise and empathy. And I do it
Search Jobs
Search Jobs
Keyword
Matching job links will appear below as you type.
Location: When autocomplete results are available use up and down arrows to review and enter to select. Touch device users, explore by touch or with swipe gestures.
Radius: Enter distance 5 15 25 35 50
Unit MILES KM
View Remote Jobs View All Jobs
View remote jobs View all jobs
Regulatory Strategy Consultant
Primary Location: United States, Remote Job ID R0000047159 Category Regulatory / Consulting Date Posted 10/16/2026
Apply Now
Success profile
About this role
Employee insights
Why Consultants work at Parexel
Learn about our culture
Overview
As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.
We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
Communicator
Detail-oriented
Problem-solver
Relationship-builder
Results-driven
Strategic
Back to nav
About This Role
About Parexel
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose -- moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart(R).
About The Role
We are seeking a Regulatory Strategy Consultant to join our team in a remote capacity. As a Regulatory Strategy Consultant, you will own regulatory strategy across significant programs and portfolios, providing leadership for major regulatory decisions, authority engagement models, and high-impact submissions. This position plays a key role in advancing clinical development through strategic regulatory planning, lifecycle management, and cross-functional collaboration. You'll work with biopharmaceutical partners to shape regulatory pathways, guide long-range development strategies, and drive submissions that bring new treatments to patients. Responsibilities include leading regulatory strategy development, managing authority engagement, overseeing high-impact submissions, and contributing to long-range development and lifecycle planning.
You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through strategic regulatory leadership and advancing clinical research. With diverse teams and continuous learning opportunities, the Regulatory Strategy Consultant can explore career paths and expand expertise across therapeutic areas and development phases.
Key Responsibilities
Own and develop regulatory strategy across significant programs or portfolios, ensuring alignment with business objectives and regulatory requirements
Provide leadership on major regulatory decisions, including authority engagement models, submission strategies, and risk mitigation approaches
Lead the planning and execution of high-impact regulatory submissions, coordinating cross-functional teams and ensuring compliance with regulatory requirements
Develop and implement long-range development and lifecycle management plans that optimize regulatory pathways and commercial outcomes
Collaborate with clinical, scientific, and commercial teams to align regulatory strategy with development timelines and market opportunities
Monitor regulatory landscape changes and provide strategic recommendations to adapt development and submission approaches
Candidate Profile
You'll Thrive In This Role If You Bring
Strengths in regulatory strategy, strategic planning, and cross-functional leadership
Extensive experience in clinical development, regulatory affairs, or a highly regulated environment
The ability to lead across teams, influence stakeholders, and communicate complex regulatory concepts clearly
A patient-focused mindset and strong attention to regulatory detail and compliance
Comfort working with regulatory databases, submission management systems, and collaborative platforms
Required Qualifications
Bachelor's degree in life sciences, pharmacy, medicine, or related field, or equivalent professional experience
10+ years of experience in regulatory affairs, clinical development, or related field
Previous experience with vaccine and/or biologic products is required
Deep knowledge of ICH-GCP, FDA and international regulatory requirements, and clinical trial processes
Experience with regulatory tracking systems, electronic submission tools, and clinical development platforms
Excellent communication, strategic planning, and problem-solving skills with demonstrated leadership ability
Preferred Qualifications
Advanced degree (M.D., Ph.D., or M.B.A.) or regulatory certification (e.g., RAC) preferred
Experience in multiple therapeutic areas or development phases
Familiarity with global regulatory frameworks and international submission strategies
Fluency in additional languages relevant to regulatory submissions
Benefits And Compensation
Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company match
Pet Insurance
For a complete list of benefits, please visit www.parexel.com/us-benefits.
Some roles may also be eligible for additional incentives, bonuses, or other compensation programs. Our Talent Acquisition team will provide details on applicable bonus plans or incentive structures for eligible positions.
We offer a comprehensive benefits package to eligible employees, which includes paid time off, a 401(k) match, life insurance, health insurance, and additional benefit offerings in accordance with the terms of our applicable plans.
If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply!
We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Back to nav
Share this job
LinkedIn
Facebook
X
Email
Employee Insights
How to describe Parexel culture in one word
Insights from Parexel employees
Watch Video
Jo on diverse project work and team culture
Jo Wang | Vice President, Technical
Watch Video
Kurt on colleagues and growth opportunities
Kurt Brorson | Vice President, Technical
Watch Video
Back to nav
Why Consultants work at Parexel
Patient-led in everything we do
We are inspired by the patients behind the data and therefore deliver first-time quality and on-time projects.
Supportive and inclusive environment
We thrive on collaboration, caring, and inclusivity - enabling our people to work together to solve complex problems and share knowledge.
Opportunities for career growth
We provide a wide range of challenging assignments, product types, geographic regions, and therapeutic areas, providing ample opportunities for learning and growth.
Flexible work arrangements
We offer the flexibility of remote work, allowing you to balance your personal and professional responsibilities while still contributing to our “We Care” team environment.
Diverse and global client exposure
We continuously learn by working with a global network of colleagues and clients to develop regulatory strategies to support their product development and approval.
Learn from experts
You will work with a team of highly experienc

Work arrangement
Yes