Farmaci/Apotek Heltid Med erfarenhet Medicinsk forskning och laboratorieverksamhet Övrigt Forskning och Utveckling Övrigt Hälsa och Sjukvård StepStone StepStone-pbs Sverige Tillsvidareanställd
Role Description| Företag |
Pfizer |
| Ledig plats |
Medical Advisor, Inflammation, Rheumatology Sweden |
| Beskrivning |
Role Description Medical Advisor, Inflammation, Rheumatology Sweden Basic Requirements: *Relevant academic degree with good scientific skills. *Preferably a Specialist in Rheumatology and/or knowledge and experience within the Rheumatology area *Preferably experience from working in the Pharmaceutical Industry *Clinical trial or research experience *Performance driven with professional demeanour and strong team-work ability *Independence and ability to work in an international setting in a matrix organization *Fluent in Swedish *Excellent social skills *Ability to travel (approx 30% of time) Responsibilities: Be medically responsible for assigned Pfizer inflammation product/products in Sweden and in collaboration with other internal colleagues from different departments identify possibilities and relevant activities to drive business. This includes, but is not limited to: To health care professionals and other external stakeholders, such as politicians and members of tender committees, disseminate information of medical relevance concerning the products of his/her responsibility and the medical implications for current practices through advisory boards, symposia and other meetings and ways of communication. By interacting with relevant health care professionals seek to stimulate research efforts to establish a wider knowledge about the products and their optimal use. Actively work for initiation of Investigator Initiated Research, Non-interventional Studies, and site selection of global company sponsored studies within the local market. Timely provide accurate and medically sound responses to enquiries by the medical society and other stakeholders concerning products within her/his responsibility. Ensure that marketing material is medically relevant as well as compliant with the regulatory requirements In collaboration with regulatory department ensure correct wording in SmPC and other documents. Provide medical expertise for formulary applications and tender processes. Make medical plans based on identified needs, and in line with country and European strategies, taking into account product life cycle. Develop and maintain a strong network of Key Opinion Leaders and other relevant external stakeholders within the assigned therapeutic area. Provide information and trainings for company colleagues from various departments. Actively participate in the Nordic Medical Affairs team and in relevant internal meetings at the European-level. Build strategic partnerships with internal collaborators, specifically Brand Managers, and therapeutic European teams and Global teams. |