Senior Global Evidence Planning Manager
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Søborg
Do you seek an opportunity to join and shape an evolving area where you can make a substantial impact? Do you want to drive development of cross-functional evidence strategies to inform development of new treatment solutions for chronic diseases? Are you skilled in navigating a complex stakeholder landscape and are you able to motivate, set direction and deliver results? Then this is your moment. A unique position as a Senior Global Evidence Planning Manager in Integrated Evidence Planning team within Global Medical Affairs (GMA) is open for a candidate with experience in strategic evidence planning. Apply now and be part of Life-Changing Careers at Novo Nordisk! The Position
As a Senior Global Evidence Planning Manager, you will become a key member of a global team of evidence planning managers from different countries and backgrounds. You will act as a strategic partner to cross-functional Global Project Teams by driving the development of cross-functional evidence strategies for diabetes, obesity and other serious chronic diseases. Key responsibilities include, but are not limited to, the following: Initiate and drive the development of cross-functional evidence strategies within assigned therapy areas and their periodic updates in collaboration with various functions, like Clinical Drug Development, Access, Data Science, Public Affairs etc. Drive the implementation of the Global Integrated Evidence Planning (IEP) Framework in collaboration with Global Project Team, GMA Medical Directors and in alignment with Operations, Regions and Affiliates Identify opportunities for further development and improvement of the GMA IEP process and connecting to other core processes with GMA and cross-functionally Align evidence strategies with other relevant functional strategies (e.g., communication strategy, medical strategy, commercial strategies) in a proactive and timely manner Proactively identify and lead opportunities for innovation and common projects within your own and adjacent business areas You will have ample opportunity to influence our deliverables, enhance our processes and identify novel ways of developing cross-functional evidence strategies. Some travel is expected (up to 20%). Qualifications The ideal candidate for this position should hold a master’s degree in a relevant field such as medicine, public health, pharmaceutical sciences, drug development, health economics or outcomes research. Formal project management training is preferred. The job requires a minimum of 5-7 years of experience in evidence planning, market access, medical affairs, commercial functions; experience within the pharmaceutical industry or consultancy. Direct experience with leading evidence planning, preferably in a cross-functional setting (payer evidence planning, GMA evidence planning, etc), will be considered as an advantage. To be successful in this position, you need: GMA/ Health Economics/Outcomes Research /Research & Development business value chain understanding Broad experience with planning and managing projects of medium- and high complexity Experience in collaborating successfully with many different stakeholders across functions and at different organisational levels, including senior level management Strong verbal and written communication skills and capability to facilitate strategy development processes and galvanize key stakeholders Fluency in written and spoken English In addition to the above, you have a high level of expertise in managing complex priorities, project management and stakeholder matrices. You have an excellent track record of successful collaboration with multidisciplinary stakeholders. As a person, you are organised, structured and have a high degree of personal self-management, as well as independence. You are comfortable working in a fast-paced and dynamic environment, you apply an innovative approach to problem solving and have outside-the-box thinking. You have a personal drive and are enthusiastic, energetic, confident and able to work on multiple tasks to meet personal and team goals - while maintaining a good sense of humour. About the Department The Integrated Evidence Planning department is part if the Global Medical Affairs area in the Novo Nordisk HQ (Denmark). The department is responsible for driving the development of cross-functional evidence strategies within a variety of therapy areas and transforming the way evidence is planned and used across the value chain. Working at Novo Nordisk At Novo Nordisk we use our skills, dedication and ambition to help people with chronic diseases and change their lives. W e don’t wait for change, we drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Altynai Satylganova at [email protected] Deadline 7 May 2023 Please note that interviews will be conducted on ongoing basis as relevant applications are received, so we encourage you to apply soon. In this role, you will be based in Copenhagen and report to the Head of Integrated Evidence Planning within Global Medical Affairs. You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to applying for this position in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
As a Senior Global Evidence Planning Manager, you will become a key member of a global team of evidence planning managers from different countries and backgrounds. You will act as a strategic partner to cross-functional Global Project Teams by driving the development of cross-functional evidence strategies for diabetes, obesity and other serious chronic diseases. Key responsibilities include, but are not limited to, the following:
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 17.4.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Forretningsudvikler
- Søborg
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