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Regulatory Affairs Consultant - FSP

Role overview

Qualifications

  • 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
  • At least 7+ years of experience in an industry-related environment with a deep Australia regulatory expertise

Responsibilities

  • Own and develop regulatory strategy across significant programs or portfolios
  • Provide leadership on major regulatory decisions, including authority engagement models and submission strategies
  • Lead the planning and execution of high-impact regulatory submissions, coordinating cross-functional teams
  • Collaborate with clinical, scientific, and commercial teams to align regulatory strategy with development timelines

Key facts

  • Remote from: Australia, Oceania, APAC
  • Freelance
  • Senior (5-10 years)
  • Medical Affairs Manager
  • English

Hard skills

Other skills

  • Communication
  • Critical Thinking
  • Problem Solving
  • Teamwork

About the company

Parexel logo

Parexel

Contract Research Organizations (CRO)

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

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

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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