Sabine Stegner

LDC Global Program Director Medical Affairs

Schwabach, Bavaria, Germany

About

Meet P3 (Powerful, Pragmatic and Passionate): Highly experienced in the area of clinical project execution/operation, project management and development of standards, guidelines and processes; More than 15 years’ experience in leading high performing teams; Ability to build collaborative relationships and to work in remote teams and matrix organizations; Strong organizational and problem-solving skills in managing multiple tasks and timelines; Experienced in leading cross functional projects and teams; Excellent communication and presentation skills; Highly motivated, hardworking, and keen to work in a regional/ global/ new environments and to improve the way we work; High knowledge of ICH-GCP; GPP, GDP, compliance and other applicable regulations;

Experience

  • Director Global Clinical Operations Compliance at BeOne Medicine
    Apr 2024 - Present · 2 yrs 3 mos

  • LDC Global Program Director Medical Affairs at Novartis Business Services
    Feb 2022 - Mar 2024 · 2 yrs 2 mos

    Part of the Lean Digital Core Team in Novartis.

  • Novartis Oncology (14 yrs 2 mos)
    • Head Medical Affairs Excellence&Governace/ Local Clinical Trial Head
      Mar 2018 - Feb 2022 · 4 yrs

      Disciplinary and professional leadership of the Department of Medical Affairs Excellence &Governance:

    • local Clinical Trial Head
      Dec 2017 - Feb 2022 · 4 yrs 3 mos

      act as local subject matter experts on all operational aspects of local sponsored studies, IIT, MAP and non-interventional trials including coordination of operational systems (e.g. CTMS, DMS, etc.)

    • Group Head Quality & Training, GMO
      Mar 2012 - Nov 2017 · 5 yrs 9 mos

      Responsible for Team Quality & Training as group leader in Trial Monitoring:

  • CRO Manager, Department ICRO (Monitoring clinical trials) at Novartis Pharma GmbH
    Jul 2006 - Dec 2007 · 1 yr 6 mos

  • Head of Clinical Supply at Novartis Pharma Production LtD
    May 2005 - Jul 2006 · 1 yr 3 mos

    Responsible for Clinical Supply Team as group leader: Management of a team of internal employees in a GMP Environment; Responsible for Storage, Packing, Labelling, Distribution and Destruction of IMPs for CPO German as local depot of clinical supply