Regulatory Affairs Consultant - Clinical Regulatory Affairs
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.
Putting Patients First—Through Regulatory Excellence
At Parexel, we are driven by a single purpose: to help patients get access to life‑changing therapies faster. As a Regulatory Affairs Consultant in a dedicated client partnership, you’ll play a critical role in making that mission real—guiding complex clinical studies through the regulatory landscape with rigor, insight, and collaboration.
This is a high‑impact opportunity for a regulatory professional who enjoys ownership, visibility, and close partnership with clients. You’ll serve as the primary regulatory expert across multiple clinical studies, working shoulder‑to‑shoulder with cross‑functional teams and client stakeholders to enable compliant, efficient trial execution.
If you thrive in a consultative environment, value strong relationships, and want your work to directly support clinical progress, this role offers the best of Parexel: scientific depth, global reach, and true partnership.
What You’ll Do:
Regulatory Strategy & Compliance
Serve as Regulatory Affairs Lead for 5+ clinical studies within a dedicated client team
Provide strategic regulatory guidance to cross‑functional study teams navigating complex and evolving global requirements
Assess regulatory impact of protocol amendments, informed consent form (ICF) updates, and other study changes
Determine whether updates are substantial or non‑substantial in accordance with applicable regulations
Advise teams on regulatory pathways, processes, and solutions for emerging trial issues
Health Authority Engagement
Plan, coordinate, and author health authority meeting requests and scientific advice packages, as required
Lead preparation and coordination of responses to health authority questions and requests for information
Manage regulatory communication strategy for assigned studies
Ensure timely and compliant submission of annual reports and safety updates
Stakeholder Partnership & Communication
Participate in regular study team meetings to track trial progress and proactively surface regulatory considerations
Provide clear and accurate updates to client management on regulatory status, risks, and upcoming milestones
Act as the primary regulatory point of contact for study teams and client stakeholders
Documentation & Project Management
Maintain accurate, current regulatory tracking systems in accordance with Parexel and client standards
Ensure all regulatory documentation meets quality expectations and agreed timelines
Support ad hoc study needs and contribute to continuous improvement and departmental initiatives
To Ensure Success, You’ll Have
At least 5 years of regulatory affairs experience to include previous clinical regulatory affairs experience
A minimum of a bachelor’s degree in a scientific or technical discipline, advanced degree strongly preferred
Knowledge of FDA Regulations and previous experience with FDA meeting requests and other packages. Experience with other global Health Authorities and applicable regulations are strongly preferred
Project management / leadership experience
Excellent interpersonal and intercultural communication skills, both written and verbal
Client-focused approach to work (Quality)
Results orientation
Teamwork and collaboration skills
Consulting skills
Critical thinking and problem-solving skills
Proficiency in local language and extensive working knowledge of the English language
Why Join Parexel?
Work in a dedicated partnership model with strong client trust and visibility
Be part of a global organization known for regulatory leadership and scientific excellence
Collaborate with talented, purpose‑driven colleagues across functions and regions
Make a meaningful contribution to clinical programs that put patients first
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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.