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Ensuring the timely generation of a wide range of clinical regulatory documents required for the development of novel therapeutic agents from discovery up until and beyond marketing approval. This includes providing hands-on scientific/medical writing
This role will be responsible for leading key post-marketing safety activities for Galderma’s approved IA/medical device products, with a primary focus on the dermal filler and biostimulator portfolio but also including additional IA/medical device
In this role, you will shape evidence and value strategies that support access to AbbVie’s immunology medicines. You will connect HTA (Health Technology Assessment) insight, asset strategy and cross-functional evidence generation to ensure plans are
Guide ICON project teams on clinical issues, ensuring studies adhere to the highest ethical principles and legal standards. Contribute to investigator meeting presentations, review study documentation, oversee safety data reviews and support Business
Accountable for the day-to-day oversight of numerous BioMarin-sponsored and collaborative studies across a therapeutic area, ensuring consistency of approach, conduct, monitoring, analysis, and reporting of studies within one or more programs.