| 126814BR | |
| Pharma | |
| Pharma - Oncology | |
| Sweden | |
| Stockholm | |
| NOV SVERIGE SWE | |
| Development & Medical | |
| Full Time | |
| Regular | |
| In accordance with BU Oncology global and Nordic strategy develop, propose and supervise the development as well as in co-operation with GMO or external CROs the implementation of clinical trials. Provide the Swedish and – for designated products Nordic - business unit with medical and scientific support enabling fast market penetrations in order to optimise growth of market share and sales, including a competitive Phase IV program. In collaboration with BU Head and Franchise Managers actively give input into the Strategic Planning process (MPH). Devise innovative, value-adding product related services for continuous improvement of satisfaction of external and internal customers. • Local product-related responsibilities and local general medical/scientific support within oncology. • Obtain or design clinical trials protocols and support these clinical trials on products selected for fast growth. This support includes, but is not limited to, assisting in investigator identification and evaluation, and at investigator meetings. • To liaise between Nordic CSO’s and headquarters/other Novartis CSO’s/regions to ensure that Danish needs for trial allocation, registration, marketing, pricing, sales arguments and in other relevant aspects are covered. Collect and forward local input to Nordic Champ and headquarters. For designated product act as Nordic representative in HQ working groups/clinical teams etc. And forward information from headquarters to all Nordic CSO’s. • To liaise with and support the GMO oncology team in the feasibility-, planning- and executional phases of clinical trials. • Develop knowledge and relations to units / KOL’s and major cooperative groups. • To assist marketing in gathering and running KOL boards. • In strategic and activity planning provide medical/scientific input to Business Unit Heads and Franchise Managers to ensure faster times to peak sales and stringent adherence to set product brand identity. Develop and implement a competitive Phase IV program and ensure that clinical trials are utilized to their full marketing potential. • Continue to develop skill sets, competitiveness and expertise of CRD and DRA, as well as marketing/sales departments’ staff on own and competitor products. • Provide Medical Information/Customer Support with medical, scientific, pharmaceutical, therapeutic and product specific information when needed. • In collaboration with the Medical Affairs Head and other MA’s and MSLs in oncology to ensure that all four Nordic countries (S, FIN, N, DK) will be sufficiently covered by the means of regular personal presence in each country and videoconferences. • Ensure that all AEs are brought to attention to the DS&E department within 24 H after receipt. | |
| MD, preferably with a Ph.D. degree and a specialty in oncology or hematology or a Ph.D. within relevant field and with relevant background. Previous experience from the pharmaceutical industry is not a request but an advantage English: fluent written & spoken Clinical and Research |
Friday, 20 September 2013
Position Title: Medical Advisor
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Sweden
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