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 Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

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22 Oct, 2026

Parexel

Statistical Programmer I

Engineering

Taiwan-Taipei

Salary not listed

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Statistical Programmer I

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Site Monitor II - FSP

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Statistical Programmer I

Job Posting Title Clinical Operations Leader / 臨床開発部クリニカルオペレーションズリーダー

Site Monitor II - FSP

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Inspector 2 - QC

Panel Service Executive

Bid &amp; Proposals Manager Brazil

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Bid & Proposals Manager Brazil

Bid & Proposals Manager Brazil