Demanda en Dinamarca (HOVEDSTADEN) de Farmacéuticos
Senior Esource Data Manager In Global Development
Clasificación del trabajo: Profesionales científicos e intelectuales : Profesionales de la salud : Otros profesionales de la salud : Farmacéuticos.
Arbejde, der forudsætter viden på højeste niveau inden for pågældende område : Arbejde inden for sundhedsområdet : Andet sundhedsarbejde : Farmaceutarbejde.
-?Biostatistics and Data Management
-?Denmark - Søborg
Are you looking to utilise your clinical data management skills in a position with global reach? Do you thrive on learning and understanding different data collection devices/systems? If so, we have an exciting opportunity which can make a difference for patients all over the world.
About the department
In Global Development, we develop new products based on proteins and peptides from early development phases to product introduction. We are responsible for managing clinical drug development worldwide securing that the processes live up to uniform global standards, regulations and business ethics. We work in global project teams and focus on delivering viable products that make a difference to patients and ultimately benefit society.
Within Global Development, Data Management (DM) Operations is responsible for clinical data collection design, flow and execution across multiple platforms and devices. The rapid advancement of technology in the health care space is making patient related possibilities endless. This is a rapidly emerging area within clinical drug development and requires the right candidate to help ensure Data Management Operations new data source/device readiness.
The position is based in Søborg, Denmark and you will be operating in a project centric organisation. You will be working closely with trial team stakeholders, suppliers and the Management team. You will have significant influence on trial design decisions and timelines. Furthermore, you will be responsible for creating and improving DM Operations standards, processes and strategic DM documents (e.g. the Data Handling Protocol) which support the integration of new data collection devices/sources. Education and training of your DM colleagues in the processes as well as the current legal, regulatory, and quality landscape is also part of your job. We expect you to keep the Management team informed regarding the adoption of new data sources/devices.
Travelling is sometimes required, <20%.
You hold a Bachelor's or a Master's degree in Natural Science or a similar degree in Medical, Nursing or Pharmacy. You are expected to have at least 4 year of experience in clinical data management and must have a good understanding of clinical drug development and GCP.
The ideal candidate is able to demonstrate solid project/stakeholder manager experience with a firm focus on risk assessment and continuous process improvement. The position requires a high level of independence, clear communication skills and an ability to consistently deliver.
You are expected to be proficient in English language both speaking and writing.
Working at Novo Nordisk
At Novo Nordisk we strive for excellence. As a world leader in in diabetes care and a major player in haemostasis and hormone replacement therapy, we are proud to make a difference for millions of people around the world. We know that results are made together, and that great opportunities for personal and professional growth are important to provide.
For further information, please contact Roland Foster on +45 3075 2817.
31 August 2017.
Servicio de empleo de origen: AMS, Servicios Públicos de Empleo, Dinamarca.
País del trabajo: Dinamarca.
Fecha de inicio: 03/08/2017.
Nº de vacantes: 1.
Nivel educativo requerido: Sin especificar.
Tipo de contrato: Jornada completa.
Duración del contrato: Indefinido.Cómo solicitar el puesto:
Empresa: Novo Nordisk A/S.
Ver las 80 ofertas de trabajo de Profesionales científicos e intelectuales : Profesionales de la salud : Otros profesionales de la salud : Farmacéuticos ofertadas.
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