Principal Consultant

2 weeks ago

Brisbane, Queensland, Australia Scendea Full time
Scendea is seeking a highly motivated individual to join our global team as a full-time Senior Consultant (CMC).
This is a hybrid position, affiliated to our Brisbane, Australia office, with a requirement to work in the office a minimum of one day per month.
This is an excellent opportunity to progress your career at a rapidly growing Regulatory Consultancy.
You will have the opportunity to play a key role in the development and mentoring of staff whilst providing high-quality regulatory technical advice and product development strategies for clients.
Role Requirements Provide strategic, technical and regulatory advice/services to clients with a special interest in CMC development of human medicinal products.
Establish and maintain a high level of technical knowledge in product development and international regulatory affairs.
Provide innovative drug development plans, data gap analyses and international regulatory strategies from a CMC perspective for complex products within the changing regulatory environment.
Contribute to technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Paediatric plans/applications, Investigator Brochures, IMPDs, Marketing Authorisation Applications, New Drug Applications, Biologic License Applications, DMFs according to area of expertise.
Lead multi-jurisdiction programs of work and deliver consulting services within your respective area of expertise.
Represent clients in regulatory agency interactions and provide regulatory solutions to agency objections.
Ensure delivery of project goals within agreed timelines, maintaining oversight of project budgets.
Lead meetings with internal and external stakeholders on matters related to any current and/or future projects, contracts, or new business opportunities.
Support Scendea's Business Development in sales/marketing introductions and generate additional business from current clients.
Line manage, train, and mentor members of the Scendea Operational team, including providing technical leadership.
Skills and Experience A high scientific calibre with a relevant science focused BSc (or equivalent), and a higher degree in a biomedical field or equivalent (e.g., a life/physical science focused MSc or preferably a Ph D).
A minimum of eight years of drug development experience.
A minimum of eight years of regulatory experience, working with TGA, FDA, and either EMA, and/or MHRA submissions, including meetings/negotiation.
Regulatory experience may include time within a National Competent Authority.
Demonstrated experience with a broad range of products, including recombinant proteins and peptides (including antibodies), prophylactic and therapeutic vaccines, biosimilar products, advanced therapy medicinal products (tissue, cell and gene therapy), RNA or DNA based products, live biotherapeutics and small molecule NCE and/or generic chemical entities.
Direct experience preferred in providing strategic regulatory planning from early-stage development up to marketing authorisation, and a proven ability to define and deliver creative scientifically driven solutions to technical development and regulatory issues.
Proven ability and willingness to lead a team and deliver education and training in chosen field, both internally, and at scientific conference presentations.
Exemplary organisational and time management skills with a high level of attention to detail, and the proven ability to work both proactively and autonomously.
High level of verbal communication and presentation skills in English, computer literacy, and competency in MS Office programs.
Willingness to work flexible hours and travel for short periods, sometimes at short notice, within the country of employment, or internationally.
The Company Scendea is an international product development and regulatory consulting group delivering market-leading scientific expertise & regulatory solutions, to advance healthcare innovation worldwide.
We are passionate about delivering strategic and operational support to clients, with a strong commitment to problem-solving and redefining customer service.
Our goal is to streamline the product development process, reduce time-to-market, and minimise overall development costs.
With a current team of over 50 staff based in the UK, Netherlands, Australia, and the US, Scendea is undergoing a period of significant growth, with the addition of new office locations and service lines to facilitate the delivery of expert and strategic global regulatory consulting services to our rapidly growing client base.
We are equally committed to making a positive impact on society by managing our environmental impacts and contributing to a low-carbon economy.
Our inclusive work culture values transparency, ethical collaboration with clients, and employee involvement in key decision-making processes, ensuring that our team is respected, supported, and engaged.
Eligibility & Conditions Applicants must reside and be eligible to work in Australia without the requirement for sponsorship now or in the future.
Closing date for applications is Monday 24th February 2025 and candidates will be notified of the outcome of their application no later than Friday 28th February 2025.
Seniority level Mid-Senior level Employment type Full-time Job function Consulting Industries Pharmaceutical Manufacturing
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