Study Manager

KIMS and ACROSTUDY Study Manager Medical Outcomes, based in Silverdal Stockholm is a department within Pfizer Endocrine Care Medical Worldwide, who collect, analyze and publish pharmacoepidemiological data on patients receiving Genotropin/Genotonorm (somatropin  rDNA originâ for injection) or Somavert (pegvisomant for injection) through established prescribing practices. The studies involved, KIGS, KIMS and ACROSTUDY are important tools within modern evidence based medicine and support physicians in optimizing the treatment of individual patients as well as contribute to a wider understanding of growth hormone and Somavert treatment. We are now looking for a Study Manager for KIMS and ACROSTUDY. The position is responsible for the overall conduct of the KIMS (Pfizer International Metabolic Database) and ACROSTUDY projects; positioning, conduct, outcomes data, quality of data and communications (www.medicaloutcomes.pfizer.com) The Study Manager is: *The operating study manager of the KIMS and ACROSTUDY projects, *The secretary of the KIMS International Board, a permanent member of the KIMS and ACROSTUDY Strategic Advisory Boards and participant in other expert groups connected to the projects *A permanent member of the Project Units, small groups of researchers conducting scientific analyses on specific topics or patient subgroups within the databases, responsible for organizing work and ensuring steady progress *A member of the Medical Outcomes Management Team *Responsible for reports published on regular basis (Annual Reports, Overviews, newsletters) *Responsible for the content on the KIMS and ACROSTUDY website *Responsible for supervising all communications from the project towards all stakeholders and channel all incoming communications for the concerned receivers *Responsible for all other production such as data to be collected, manuals, national package of analysis, patient reports etc. The Project Manager will cooperate closely with the team managing and providing the collection tools. *Responsible for supervising the conduct of the projects in all participating countries (Responsible for the education and training of local managers, monitors, personnel within the department and other stakeholders). This includes lecturing, teamwork and production of teaching materials and requires stable and efficient cooperation with different parts of Pfizer at country, regional and global levels *Responsible for handling all documents within the project in accordance with the routines devised by Pfizer internal SOP *Responsible for initiatives and actions to improve the data quality i.e. planning, implementation and exercising. The position is located in Sollentuna, Sweden. We look for a person who has: *Working experience: * in study management *of post marketing studies / research databases *in international environment *skills in communications with the health care professionals and key customers *good interpersonal skills *good command of English both written and oral *a medical background preferably in endocrinology The applicant should be: *cooperative *responsible *willing to travel *team-oriented *well-organized with a high degree of flexibility *goal-oriented with analytical skills *open-minded and job-committed *open for challenges and able to work under stress We offer an interesting and challenging job in the international environment and in a friendly team of 17 employees with multiple interactions w