Dr. Annalisa Macagno

Angestellt, Senior Project Manager, Tecan Group Ltd.
Zurich, Switzerland

Fähigkeiten und Kenntnisse

Project management
In vitro diagnostics
Drug Discovery
Business strategy
Cross-functional Team Leadership
Assay Development
Product Development
Monoclonal Antibodies
Immunology
Oncology
Cell Biology
Molecular biology
Intellectual Property

Werdegang

Berufserfahrung von Annalisa Macagno

  • Current 1 year and 5 months, since Jan 2025

    Senior Project Manager

    Tecan Group Ltd.
  • 4 years and 6 months, Oct 2020 - Mar 2025

    Senior Project Manager, QM & RA (part-time)

    Effectum Medical AG
  • 2 years and 5 months, May 2022 - Sep 2024

    Global Project Manager (part-time)

    Roche Diagnostics International AG, Schweiz

  • 3 years and 8 months, May 2020 - Dec 2023

    Strategy & Planning Advisor

    Project-base

    • Supporting the development of business strategies through evaluation of technologies, due diligence investigations, analysis of market and competition, and scouting of strategic alliances • Supporting the design of business plans with analyses of value creation, definition of milestones, preparation of project plans and design of exit strategies

  • 1 year and 6 months, Dec 2018 - May 2020

    Head of Science

    Proteomedix AG

    • Responsible for strategy development for new products (identifying new biomarkers, indications and technological platforms for new business opportunities in oncology). • Evaluating competitive positioning, developing market entry strategies and providing decision support to top management for business development and product launch. • Establishing biomarker plans, organising resources and managing portfolio of projects to qualify new biomarkers scientifically, technically and clinically.

  • 3 years and 4 months, Aug 2015 - Nov 2018

    Head Assay Development

    Proteomedix AG

    • Led and managed portfolio of projects in oncology from biomarker selection to CE mark of IVD product. • Prepared and managed budget, reporting directly to CEO. • Led multi-disciplinary teams (research, regulatory, supply & manufacturing, clinical, medical affairs, commercial) for product development. • Supervised and coached the project team (3 direct reports), liaised KOL, managed external partners and CMOs. • Implemented compliance to regulatory requirement (ISO 13485) and managed risks.

  • 4 years and 9 months, Aug 2011 - Apr 2016

    Scientific and Busines Advisor

    Redbiotec and Redvax

    • Analysed market opportunities and intellectual property landscape and supported management to define business strategies and project goals. • Integrated scientific research project proposal into a cost effective business plan for the preclinical development of a novel vaccine candidate for HSV. • Provided advise for the development of a preclinical cytomegalovirus vaccine candidate out-licensed to Pfizer and contributed to the creation of a proprietary technology platform for the design of vaccines.

  • 2 years and 1 month, Dec 2011 - Dec 2013

    Head Antibody Discovery

    ImmunoQure Research AG

    • Set up company’s activities from inception until full capacity business, supporting the board to define goals and select projects (autoimmunity/inflammation). • Planned, managed and directed execution of all projects (budget, monitoring of prpogress to reach milestones). • Coordinated a cross-functional team of 30 experts (13 scientists and group leaders, 5 direct reports) at 6 international locations for advancing 4 programs to full pre-clinical characterization.

  • 1 year and 8 months, Apr 2010 - Nov 2011

    Senior Scientist, Immunology

    CT Atlantic AG

    • Provided input in cancer immunobiology • Managed an oncology project and supervised the antibody technology team for the development of 8 lead antibodies for use in passive therapy or in combination with vaccine (subject of patent application WO 2012 / 163771). • Doubled the efficiency of cell technology and improved its robustness by successfully establishing quality assurance procedures. Cut down to 1/3 the time required for molecular cloning and complete sequence identification.

  • 2 years and 7 months, Sep 2007 - Mar 2010

    Staff Scientist

    Institute for Research in Biomedicine

  • 5 years and 5 months, Apr 2002 - Aug 2007

    Research Scientist (Postdoc)

    Institute for Research in Biomedicine

  • 3 years and 6 months, Oct 1998 - Mar 2002

    Doctoral Student

    Research Department of the Cantonal Hospital, St Gallen

Ausbildung von Annalisa Macagno

  • 1 year and 6 months, Jan 2015 - Jun 2016

    Business Administration (MBA)

    University of Rochester

  • 1 year and 6 months, Jan 2015 - Jun 2016

    Executive MBA (EMBA)

    University of Bern

  • 3 years and 6 months, Oct 1998 - Mar 2002

    Biochemistry

    University of Zurich (Switzerland)

    Biochemistry / Immunology

  • 5 years and 7 months, Sep 1991 - Mar 1997

    Biological Sciences, Biochemistry

    University of Trieste (Italy)

    Biomolecular orientation, Biochemistry

Sprachen

  • English

    C1 (Fließend)

  • Italian

    C2 (Verhandlungssicher / Muttersprachlich)

  • German

    B1-B2 (Gute Kenntnisse)

  • French

    A1-A2 (Grundkenntnisse)

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