Rosine Buxtorf Mucklow

Professional Activities

  • Creation and management of new and existing SOP and QA documentation
  • Assurance of GCP compliant documentation of clinical trials under the responsibility of PMU and MedRes
  • Contribution to GCP trainings organized by MedRes
  • Performance or contribution to clinical trial audits

Higher Education & Qualifications

  • Master thesis in parasitology under the supervision of Prof. Dr. N. Weiss at the Swiss Tropical Institute in Basel; Topic: Shistosomiasis
  • Degree studies in biology at the University of Basel, Switzerland

Work Experience

  • 2001 - 2002: Clinical Research Scientist, Novartis Pharma AG, Basel
  • 2002 - 2004: Clinical Development Scientist, Tillotts Pharma AG, Ziefen
  • 2004 - 2005: Clinical Trials Manager, F. Hoffmann-LaRoche Ltd., Basel
  • 2005 - 2007: Quality Assurance Officer, PMU, SCIH, Swiss Tropical Institute, Basel