International Trial Manager in Trial Operations and Obesity
Contrato en HOVEDSTADEN (Dinamarca) de Directores de políticas y planificación
Clasificación del trabajo:Directores y gerentes : Directores administradores y comerciales : Directores de administración y servicios : Directores de políticas y planificación. Ledelsesarbejde : Ledelse inden for administration og erhvervsorienterede funktioner : Ledelse inden for forretningsservice og administrative funktioner : Ledelse inden for virksomhedsstrategi/policy området.
Descripción de la oferta de trabajo:
-?Clinical Trial Management -?Denmark - Søborg Obesity “We have an open and respectful environment, where we challenge each other, welcome new ideas and inspire each other to develop”. Our area is characterised not only by interesting Non-Interventional Study (NIS) and phase 2 to 4 trials but also by the dedication to our mission statement, part of which is referenced above. In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to product introduction. We ensure medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to uniform global standards, regulations and business ethics. About the department In Trial Operations, Obesity we are approximately 30 highly skilled and ambitious employees. We are responsible for the planning, execution and finalisation of clinical trial activities in phase 2-4 within the obesity portfolio. We collaborate closely with other functional areas, Contract Research Organisations and our colleagues worldwide. We value an open team and trust-based working environment. Our working environment is characterised by interesting and complex assignments and continuous professional development opportunities. The position You will be part of the International Study Group and ensure coordination of trial management activities in a proactive way through clear communication and teamwork skills. Organising and executing team meetings as well as planning, preparing and presenting at Global Investigator and monitor meetings are also part of your responsibility. You have a structured and analytical approach as well as a high quality mind-set when developing trial documents such as protocols, monitoring guidelines, recruitment and retention strategies, risk management plans, communication plans etc. You sense the importance of detail when setting up a trial and providing input to clinical IT systems. At the same time, you are able to digest complex data output and evaluate the level of data quality during a trial. You are able to ensure progress of trial activities within given timelines and in accordance with the trial budget. Qualifications You hold a university degree in Natural Science or equivalent with experience in trial management as well as clinical trial methodology. You have solid project management/leadership skills and work in an independent manner. You must have the drive and focus to meet challenging deadlines and know how to prioritise between different tasks in a dynamic environment. You are a dedicated team player with a high degree of flexibility and cross-cultural awareness who inspires trust amongst colleagues and partners. Proficiency in written and spoken English is essential. Working at Novo Nordisk At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Lone Petersen at +45 3075 0947 or Arne Christensen at +45 3075 6053. Deadline 18 August 2017.
Servicio de empleo de origen:AMS, Servicios Públicos de Empleo, Dinamarca.