Telix Pharmaceuticals Limited
Telix Pharmaceuticals Limited
501 – 1,000 Employees
BiotechnologyConsultingHealthcare

Telix Pharmaceuticals Limited is a commercial-stage biopharmaceutical company developing and commercializing theranostic radiopharmaceuticals for cancer and rare diseases. Its approach combines targeted imaging with radiation-based treatment to support more informed clinical decisions and personalized care.

The company’s pipeline spans prostate and kidney cancer, neuro-oncology, and musculoskeletal cancers. Telix has secured global regulatory approvals for its lead imaging product, Illuccix®, and continues to advance a broad program of clinical trials worldwide. Its team works across healthcare, biotechnology, and related commercial disciplines to bring radiopharmaceutical innovations from development into clinical use.

Regulatory Affairs Manager, Advertising & Promotion – Telix Pharmaceuticals (Remote)

Lead advertising and promotion compliance for Telix’s radiopharmaceutical products in cancer and rare-disease care. Review global materials, support FDA submissions, and shape regulatory strategies.

Description

  • Advise on regulatory requirements for advertising and promotional materials supporting investigational and approved commercial products
  • Lead regulatory reviews of advertising, promotion, disease-awareness, training materials, campaigns, and launch strategies
  • Evaluate materials for the United States, Canada, Australia, the United Kingdom, Belgium, the Netherlands, Luxembourg, Spain, Germany, and other markets outside the United States
  • Represent Regulatory Affairs on the Materials Review Committee alongside Medical Affairs, Legal, and Marketing
  • Coordinate health authority submissions, including U.S. Form FDA 2253 filings
  • Track U.S. promotional regulations, FDA guidance, enforcement activity, and industry developments
  • Prepare, maintain, and archive abbreviated Prescribing Information (aPI)
  • Act as the regulatory contact for global, regional, and local brand teams
  • Oversee promotional and non-promotional material reviews across priority international markets
  • Help affiliates apply national and regional codes, including EFPIA, ABPI, Farmaindustria, and AKG/IFPMA
  • Coordinate external vendors and uphold consistent global review procedures
  • Build cross-functional partnerships that support compliant communication strategies
  • Drive improvements to processes, best practices, and tools for advertising and promotion compliance

Requirements

  • Bachelor’s degree in life sciences, law, public policy, or a related discipline
  • At least five years of pharmaceutical regulatory affairs experience, including two or more years focused on advertising and promotion
  • Experience reviewing U.S. advertising and promotional materials and preparing Form FDA 2253 submissions
  • Thorough knowledge of applicable international, national, and regional regulatory frameworks, processes, and requirements
  • Familiarity with Veeva PromoMats is preferred
  • Clear and effective communication skills
  • Ability to work productively with cross-functional partners
  • Demonstrated commitment to ethical conduct
  • Adaptability in a changing work environment
  • Dedication to ongoing learning and professional development

Benefits

  • Annual bonuses tied to performance
  • Equity-based incentive plan
  • Generous vacation allowance
  • Paid wellness days
  • Learning and development support
  • Competitive compensation

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