Associate Director, Global Regulatory Affairs
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Associate Director, Global Regulatory AffairsGenève, Geneva, Switzerland Updated: Thursday 9 January 2025
Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.
See Yourself at TelixThe Associate Director, Global Regulatory Affairs is primarily responsible for ensuring regulatory objectives are met and align with Telix’s corporate objectives. This person is responsible for the execution of global regulatory strategy and dossier compliance within Telix specifically for assigned products.
Key Accountabilities:- Prepares and executes, in collaboration with other regulatory affairs team members, global regulatory strategies and submission requirements pertaining to assigned projects in line with Telix’s objectives and initiatives.
- Represents regulatory affairs on project teams as a subject matter expert by providing guidance and regulatory expertise to other departments in support to product development.
- Leads regulatory agency interactions including, but not limited to, coordination of redaction of briefing package, preparation of meeting minutes and responses to agencies questions.
- Prepares, reviews, analyses, and consolidates all relevant pharmaceutical and related technical information required for regulatory submission of the company's (investigational-) medicinal products with regulatory agencies (ODD, PIP/PSP, Scientific advices, IND/CTA, BLA/MAA).
- Provides regulatory assessments for change management and ensures compliance of the regulatory submissions by filing and/or coordinating regulatory amendments in relation to the change, where applicable.
- Monitors global health authority regulations, guidelines, and specifications including FDA, EMA, Health Canada, Therapeutic Goods Authority to maintain regulatory submission compliance.
- Leads regulatory interaction with health authorities for IND and BLA filings (or equivalent).
- Undergraduate degree in a scientific field (chemistry, biology, pharmaceutical sciences) required; Advanced degree preferred.
- 7+ years’ experience in regulatory affairs for pharmaceuticals products.
- Direct experience in writing regulatory sections for global health authority applications (i.e., IND/IMPD, BLA/MAA).
- Direct experience in Radiopharmaceuticals, biologicals, and/or clinical preferred.
- Experience across product development to Marketing Authorization.
- Comprehensive knowledge of drug development process, biopharmaceutical technology, drug manufacturing processes, GMP and related issues.
- Ability to understand and interpret any regional regulations and guidance documents as well as common and scientific publications.
- Experience working globally in the US and EMEA.
- Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected.
- Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges.
- Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do.
- Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results.
- Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders.
- Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges.
- Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language.
- Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals.
- Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges.
- Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills.
At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.
Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
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