• Co-responsible Clinical Pharmacology Scientist

    at Novo Nordisk

    April 2018 - September 2018

    Region Sjælland

    • Participation of 2 clinical pharmacology trials, including co-design of 1 protocol • Compilation of study documents, including ICF and contracts • Management of external collaborations with CROs and central labs. • Initiation of investigators meeting and participation site selection visits • Review and control of data quality prior to Data Base Lock • Cross-functional collaboration with internal external stakeholders

  • Clinical Research Associate

    at Novo Nordisk

    May 2013 - October 2015

    Shanghai Shi

    • Preparation of country level’s protocol, ICF, patient diaries, etc. • Organization of investigator and project meetings • Writing and processing blood sample export application • Management of Third-party staff • Conducting site visits and reporting visits findings

  • Clinical Research Associate

    at IQVIA

    August 2011 - April 2013

    Shanghai Shi

    • Site management from trial initiation to trial closure • On-site quality control of the data • Ensuring compliance with GCP, protocols, and regulations


  • PhD candidate

    at Aarhus University

    2016 - at Present (4 years) Region Midtjylland