Oferta en Dinamarca (HOVEDSTADEN) de Directores de políticas y planificación
Senior International Trial Manager For A Cardiovascular Outcomes Trial
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 Do you want to be part of a team leading large global clinical trials to develop the world’s best diabetes treatments? And do you like to work as a project manager with many stakeholders? Then a job as Senior International Trial Manager might be just the right job for you. 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, Semaglutide Diabetes & Diabetes Outcomes, we are approximately 75 highly skilled and ambitious employees. We are responsible for the planning, execution and finalisation of clinical trial activities. Further, we collaborate with external vendors and our colleagues in the Novo Nordisk affiliates worldwide. The position In the job as Senior International Trial Manager you will work on a large global Cardiovascular Outcomes trial. The job demands that you are capable of directing and driving activities within global clinical trials. You will be responsible for ensuring that project key deliverables are met in time, are of high quality and within budget. You will be part of driving the international study group where you will contribute to planning and conducting team meetings with focus on stakeholder engagement, knowledge sharing and decision making. The job requires a structured and analytical approach during development of relevant trial documents such as trial protocol, informed consent, recruitment strategies, risk analysis plans, communication plans and trial budgets. Qualifications You hold an academic degree within life science or healthcare. You have knowledge of clinical trial planning, execution and/or finalisation. Further, you have experience in ensuring that your stakeholders deliver their best in an ever-changing environment. The job requires proficiency in English. You work independently while also being a dedicated team player and have good cross-cultural skills. You are detail-oriented, while able to maintain overview, digest complex data and evaluate the adequate level of quality. Due to the summer holiday we expect to conduct the interviews in August. 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 Hani Yassin at +45 3079 0281 or Janne Ulbak at +45 3075 4450. Deadline 2 July 2017.
Servicio de empleo de origen:AMS, Servicios Públicos de Empleo, Dinamarca.