Norway
An experienced medical affairs professional with a track record of high work capacity, and proven ability to successfully deliver results within medical affairs. I have been managing small teams at in-country and above country level and worked in a matrix organization with cross-functional groups internally in Norway and across multiple European markets. To me medical affairs is crucial in supporting market strategies with scientific focus and knowledge and customer insights into successful strategy and tactical execution. I have a good understanding of the pharma business environment and can strengthen the organisation both by challenging and supporting commercial teams with the medical voice. Pharmacist proud of working in pharma, as a great contributor to people's health. I really believe we make a difference in people's lives, and my role in medical affairs is to make sure our activities are focused on the patients and their medical needs, and develop better solutions for patients and healthcare.
Leading the innovation medical affairs group for Viatris in Europe, including cMSL team. Focusing on the innovation phase III medical affairs activities within therapeutics areas lupus and cardiovascular disease, respectively.
Medical lead UK, Norge og Danmark
Medical lead for the subcluster
Sub-Cluster medical lead for Nordics, Ireland, Switzerland and Austria in Upjohn
In my role as medical advisor I was developing and executing the country medical plan that supports the strategic operating goals for the EPBU business, and was the single country point of accountability for medical and scientific initiatives related to the EPBU portfolio of products. Responsibilities in this role includes work to; o Develop and execute a medical strategy that supports the country operating plans with a specific focus on driving business growth through medical insights; ie portfolio maximization and local business development initiatives. o Provide subject matter expertise and strategic leadership on business development,supplemental submissions and rapid response teams o Provide medical leadership on EPBU EU regional and global projects and strategies as required. o Serve as key country point of contact in developing country-based Medical Information strategies o Act as the single point of accountability for medical knowledge and insight at a country level during the transition of LOE products. o Provide medical guidance and input to commercial and regulatory in support of key product maintenance activities and product defense o Oversight responsible for all regulatory and safety activities related to the portfolio of products o Provide a critical review and medical input into promotional materials