Telix Pharmaceuticals seeks a Manager, Regulatory Affairs (Clinical Labeling) to develop, maintain, and oversee IMP labeling for global clinical trials. You will ensure compliance with GMP, GCP and country-specific requirements while supporting supply chain timelines.
You will partner with Regulatory Affairs, Clinical Operations, Quality and external vendors to manage labeling documents, translations, and version control across regions including the US, EU, UK, Canada and Asia-Pacific.
#J-18808-Ljbffr
📌 Global Clinical Labeling Manager (IMP) – Hybrid (Australia)
🏢 Telix Pharmaceuticals (AMER)
📍 Australia
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.