Global Medical Affairs Director, Autoimmune Diseases

Novartis UK

London, United Kingdom
Hybrid
Global medical affairs programs
Innovative evidence generation
Launch readiness and post-market solutions
The Global Medical Affairs Director develops and implements strategic and operational Therapeutic Areas (TAs) Global Medical Affairs programs, focused on innovative evidence and launch readiness along with post-market solutions

Job Summary

  • The Global Medical Affairs Director develops and implements strategic and operational Therapeutic Areas (TAs) Global Medical Affairs programs, focused on innovative evidence and launch readiness along with post-market solutions.
  • They address and deliver strategic pre-launch and launch medical activities needs for patient, clinical, access and value to health care systems.
  • The role involves leading medical-scientific input for studies, serving as a disease-area expert, and co-developing Brand/Franchise Medical Affairs strategy.

Matching Summary

The Global Medical Affairs Director develops and implements strategic and operational Therapeutic Areas (TAs) Global Medical Affairs programs, focused on innovative evidence and launch readiness along with post-market solutions.

Skills & Requirements

Must-have

  • Global Medical Affairs programs
  • Innovative evidence generation
  • Launch readiness and post-market solutions
  • Medical/scientific engagement strategy
  • Integrated Evidence Plan (IEP) execution
  • Disease-area medical and scientific expert

Nice-to-have

  • Critical thinker
  • Agile mindset
  • Navigate uncertainty
  • Collaborate across functions and markets
  • Delivery focus for time and quality
  • Innovative, multichannel communication formats

Key Requirements

  • Medical Degree (MD)
  • Specialist Degree or qualification in Rheumatology
  • Pharmaceutical Industry experience in Medical Affairs
  • Global level experience
  • Clinical Development firm experience
  • Firm knowledge of Clinical Trials, GCP
  • Scientific and clinical methodology
  • Protocol designs, management
  • Regulatory requirements for clinical studies
  • Deep understanding of healthcare systems
  • Key external stakeholder understanding

Work Rights

Not specified

Tailored Resume

Cover Letter