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Senior Regulatory Affairs Consultant / Regulatory Project Lead

United States of America, Remote Additional Locations: Remote - United States of America Job ID R0000007861 Category Regulatory / Consulting Date Posted 03/10/2023
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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

About This Role

If you are passionate about innovative therapies, love leading complex regulatory filings, and live for quality, on time, and within budget project deliverables, Parexel is E-X-P-A-N-D-I-N-G and we currently have openings for Senior Regulatory Affairs Consultants / Regulatory Affairs Leads. These are incredible opportunities to join a tight knit team of amazingly nice and extremely experienced colleagues!

As a Senior Regulatory Affairs Consultant / Regulatory Project Lead you will provide leadership to highly experienced project teams and manage the day-to-day operations and complexities of preparing and filing NDA and/or BLA applications. You will strive to achieve operational excellence through on time delivery that is within budget and to the highest quality with the goal to exceed client expectations.


Successful candidates must, at minimum, possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at least 10-15+ years' experience working in a similar capacity leading US FDA filings within a CRO, Biotech, or a Pharmaceutical Company (previous CRO or Consulting firm experience is highly preferred).  Past experience overseeing a cross-functional team involved in the creation of US Regulatory Filings to include NDAs and/or BLAs is required. Previous vaccines experience is a plus!

This position also requires experience in project scheduling, managing resources and budgets, coordinating team activities, as well as experience in Regulatory Affairs related activities.

Successful candidates must also possess the following:

•The ability to build and sustain relationships
•Critical thinking and problem solving
•The ability to influence and lead teams
•Financial management skills
•Strategic thinking skills
•Attention to detail and commitment to quality
•Conflict management skills
•Consulting skills
•Contingency planning and risk management skills
•People management skills
•Excellent interpersonal, verbal and written communication skills
•Client focused approach to work
•A flexible attitude with respect to work assignments and new learning
•Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
•Proficient in Microsoft Excel, Power Point, MS Project and Word.
•Willingness to work in a matrix environment and to value the importance of teamwork.
•Experience with financials and managing project budgets

Up to approximately 10-15% Domestic and/or International Travel may be required in the future.


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.

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