Regulatory Affairs Consultant - FSP

Parexel · Australia

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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


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