Regulatory Affairs Consultant - Labelling

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Hiring Remotely in Ryde, New South Wales, AUS
In-Office or Remote
Pharmaceutical
The Role

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.

Labelling specific expectations:

• Previous experience working in industry in support of Global Labeling, Regulatory (Clinical / Safety), or Medical Writing for labelling updates

• Use of document management tools (internal systems) and external platforms

• Strong familiarity with the Company Core Datasheet (CCDS) and its implementation into labelling and artworks

• Knowledge of the triggers that lead to a CCDS update, and ability to manage/coordinate impact assessments for technical changes impacting labelling

• Understanding of Safety Signal Management and the impact of confirmed safety signals on labelling

• Familiarity with CCDS governance processes in Pharma Companies

• Some understanding of Periodic Safety Update Reports (PSUR) and potential impact on labelling

• Appreciation of the relationship between labelling and artwork processes

• Understanding of the regulatory processes required to update labelling of a product e.g different variation categories

• Familiarity with the Addendum to Clinical Overview (Module 2.5) and its preparation to support a labelling variation.

• Some appreciation of the Regulatory requirements for labelling updates in different regions e.g. EU, EAEU, US and APAC.

• Knowledge of local labelling requirements .

• Review and approve promotion and advertising materials, medical education, and social media content in accordance with approved labelling and clinical materials. Participate in the promotion review committee and provide regulatory guidance in accordance with local market requirements.

Overarching project expectations:

  • Demonstrates the use of the organization’s consulting models and methodologies and uses experience to suggest possible developments/improvements

  • Provides a full range of technical and/or business consulting services within personal area of expertise dealing mainly in areas where policy or precedent is clear

  • Completes activities within project scope and objectives in a timely manner with an understanding of issues which may impact project profitability, quality, and client satisfaction

  • Facilitates client decision making by framing issues, presenting options and providing objective business advice

  • Collaborates with colleagues, as needed, to discuss and facilitate resolution of problems or conflicts. Provides guidance as needed to lower level colleagues on appropriate methods of executing project activities

  • Acts as a trusted advisor to clients and/or project team on technical and/or process issues

  • Supports development of business solutions addressing specific client needs using best practices and knowledge of the client’s business and key industry drivers

  • Interacts professionally at multiple levels including senior management within a client organization

  • Facilitates clients in identifying and addressing their needs and develops processes and solutions to address issues before they become significant problems

  • Completes basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, project deliverable archiving, participation in internal initiatives/projects or as a mentor as requested by management

  • May participate in thought leadership activities (i.e. present speeches or seminars to industry groups and/or author articles.)

Requirements:

• Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline, Advanced Degree Preferred

• 8 years + experience in an industry-related environment, inclusive of 2+ years of labeling/regulatory experience combined with other global responsibility from Australia including New Zealand.

• 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

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The Company
HQ: Durham, North Carolina
20,524 Employees

What We Do

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.

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