Reporting to the CMR Director, you will be responsible for the operational excellence in CMR, alignment of functional objectives with Region Europe and Corporate priorities, tracking KPIs and ensuring excellence in execution for Medical Education, Medical Affairs and broader CMR deliverables. You will support the planning, execution and reporting of the CMR activities, such as AMP process, KOL engagement and Individual engagement plans, Educational activities, publication planning, reporting of Medical activity to NNRE/HQ, managing providers of outsourced activities, reporting of Clinical activities, etc.
Your main responsibilities will be focused on:
Annual and longer term strategic planning for CMR, aligned with Global and RE strategies priorities. To ensure CMR Operations achieves its targets efficiently in accordance with internal SOPs, external requirements and full compliance to Business Ethics. Management of CMR defined projects, budget management for defined CMR projects and internal reporting within the department. Management of cross-functional KOL engagement planning process, tracking and ensuring high quality execution of scientific dialogue. Support Academic and professional organisation collaborations. Support efficiency projects across CMR. Ensure supervision of relevant systems such as DXD, Zinc Map . Ensure RMA customer lists in SELAS are aligned with influence mapping results and product brand plans, monitoring and reporting RMA KOL and HCP interactions in SELAS. Provide project leadership and supervision for ad hoc projects.
We are a Great Place to Work. Come to work with us!
At Novo Nordisk, we use our skills, dedication and ambition to help people with chronic diseases. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.
Requisitos del candidato
De 1 a 3 años
- You hold an academic degree in Business or Life Science. - Post-graduate qualification in business and management is desirable. - At least 3 years’ experience within the pharmaceutical industry in a project management role. - Valuable experience managing significant medical/scientific programs and budgets - Mastery of MS Office Suite (Word, Excel and PowerPoint) - Fluent in English and Spanish.