Telix Pharmaceuticals (AMER)

Likely evergreen RemoteNorth America

Global Regulatory Affairs - CMC Talent Community

United States

Writes and manages CMC regulatory dossiers (e.g., Module 3) for radiopharmaceutical and biopharmaceutical products, ensuring compliance with global standards like ICH and FDA/EMA guidelines.

Regulatory Compliance Technical Writing Veeva

Open 93d RemoteNorth AmericaC-level

VP, Medical Affairs Americas

United States

Leads medical strategy and execution for radiopharmaceutical products in the Americas, guiding clinical trials, KOL engagement, and product launches while managing a team of medical directors.

Veeva

Open 25d RemoteNorth America

Manager, Regulatory Affairs (Ad-Promo)

United States

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…

API Veeva

Regulatory Compliance Technical Writing Veeva

Manager, Regulatory Affairs (CMC)

Open 25d North America

Canada

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…

Open 23d RemoteNorth AmericaContract

Manager, Regulatory Affairs (Clinical Labeling)

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…

GCP Regulatory Compliance Veeva Version Control