Project Management has always been a key function of my different roles in the pharmaceutical industry. I have gained extensive experience in

  • Project, process and people management
  • Medical assessments /evaluations of projects
  • Coordination of product development
  • Collaboration with research and regulatory teams
  • Liaison with external vendors as needed

Research & Development activities are among my favorite tasks. Patient care and improvement of treatment options are my commitment. I support you in:

  • Planning, design, and implementation of clinical development plan
  • Preparing BASEC /  Health Authority submissions of research projects
  • Supervision of clinical program (all phases)
  • Coordination of sponsor, study teams, clinical trial units etc.
  • Organisation of investigators’ meetings

I like to share the skills I have gained in
Regulatory Affairs along with my dedicated expert team.

We provide support in:

  • Scientific advice meeting
  • Pre-submission meeting

Preparation and/or review of:

  • Marketing authorisation applications (all modules)
  • Orphan drug designation applications

My former position as Head of Medical in supervising Medical Affairs is helpful to support you with:

  • Medical / scientific writing or reviewing (DE/EN)
  • Interviews or congress reports (DE/EN)
  • Preparation or reviewing of educational or promotional materials
  • Organisation of satellite symposia, lecture tours, advisory boards
  • Key opinion leader management and education