Clinical Project Manager in Global Development. HOVEDSTADEN
Oferta de trabajo de Directores de administración y servicios en HOVEDSTADEN (Dinamarca)
Clasificación del trabajo:Directores y gerentes : Directores administradores y comerciales : Directores de administración y servicios : Directores de administración y servicios no clasificados bajo otros epígrafes. Ledelsesarbejde : Ledelse inden for administration og erhvervsorienterede funktioner : Ledelse inden for forretningsservice og administrative funktioner : Ledelse inden for anden forretningsservice og andre administrative funktioner.
Descripción de la oferta de trabajo:
-?Clinical Trial Management -?Denmark - Søborg Are you motivated by the opportunity to setting up and driving global clinical programmes and do you want to exert your influence by leading project teams to develop the world’s best haemophilia treatments? Do you thrive by working in an international environment and are you prepared to join an area with a high level of awareness and attention? Then we may have just the right job for you. In Trial Operations, Biopharm we are looking for a new colleague to join us working as a Clinical Project Manager (CPM). This is an exciting opportunity to increase your experience within clinical project management and to develop your competencies within a study life cycle ranging from planning and preparation through execution to finalisation of our clinical trials. 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 Trial Operations, Biopharm, a part of Global Development, is a team of 75 highly skilled and ambitious colleagues responsible for planning and execution of clinical trial activities in accordance with the Product Development Plans within haemophilia, rare bleeding disorders and growth hormone. The scope of our activities is phase 1 to 4 clinical trials and non-interventional studies in collaboration with our Novo Nordisk affiliates. Our environment is characterised by a vast global network with challenging assignments in a project centric organisation. We focus on continuous personal and professional development and exciting opportunities which arise when working for a large headquarter function. The position As a CPM, you are responsible for engaging, directing and co-driving a global clinical programme from an operational perspective. You will ensure that project key deliverables are met on time at a high quality and within budget by using your extensive project leadership as well as operational trial management knowledge. You are expected to inspire better practices as well as create improvements while at the same time support a number of trial management teams to ensure progress, coordination and clear communication across skill areas. You are expected to create a great team spirit by contributing to a positive, challenging and inspiring working climate. In addition to the assigned program, you will have opportunities to participate in cross-project/cross-functional tasks forces and improvement project in order to continuously strengthen Trial Management. Last but not least we expect that you will act as trainer across our project teams and mentor new staff. Qualifications You hold a university degree in Biological, Medical or Pharmaceutical Science or equivalent and have at least 5 year of trial management experience and a proven track record of all operational aspects of planning, initiation, conduct and finalisation of clinical trials. Project Management experience is a must. You are a dedicated team player who motivates your team to deliver their best in an ever-changing environment. You know how to prioritise between different tasks in a dynamic environment which requires a high degree of flexibility. By use of clear communication and strong presentation skills you inspire trust among your colleagues as well as your stakeholders. You have excellent cross-cultural awareness and like to contribute to cross-functional work. Working at Novo Nordisk We combine world-class scientific, pharmaceutical and clinical expertise with the highest ethical standards to improve the quality of life for millions of patients. That is why we trust you to make a difference by doing your best. Contact For further information, please contact Ulrika Qvint at +45 3075 4640. Deadline 13 Aug
Servicio de empleo de origen:AMS, Servicios Públicos de Empleo, Dinamarca.