Regulatory Affairs Consultant - FSP
Parexel
Australia-North Ryde-RemotePosted 1 day agoDiscoveredMatch locked
RemoteFull time7+ years exp
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.
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
Not included in the source posting: about the role, what you'll do, benefits.
Who can apply
The employer didn't state any visa, work authorization, citizenship or clearance requirements in this posting. Confirm with the employer before applying.
Read automatically from the employer's posting text. Always confirm with the employer — requirements can change after a job is published.