I contribute to clinical research with expertise and empathy. And I do it
Regulatory Affairs Consultant - FSP
Primary Location: Australia, Remote Job ID R0000046844 Category Regulatory / Consulting Date Posted 10/19/2026
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
About This Role
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
Key Requirements
- Significant Regulatory Affairs experience supporting Australian product development and lifecycle management.
- Proven experience leading or supporting HA interactions and regulatory procedures.
- Strong understanding of Marketing Authorisation Applications (MAAs) and CTD/eCTD dossier requirements.
- Experience preparing and reviewing regulatory documentation, including Module 1 content and health authority briefing materials.
- Demonstrated expertise in regulatory strategy development, dossier review, and health authority engagement.
- Excellent project leadership, stakeholder management, and communication skills.
- Ability to manage multiple regulatory priorities while delivering high-quality outcomes in a fast-paced environment.
Skills:
- Project management knowledge
- Client-focused approach to work
- Results orientation
- Teamwork and collaboration skills
- Consulting skills
- Excellent interpersonal and intercultural communication skills, both written and verbal
- Critical thinking and problem-solving skills
- Proficiency in local language and extensive working knowledge of the English language
Knowledge and Experience:
- At least 7+ years of experience in an industry-related environment with a deep Australia regulatory expertise
Education:
- Minimum of a Bachelor’s Degree in a Scientific or related area of study
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