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IWRS Coordinator in CMC Development. HOVEDSTADEN. Dinamarca

Oferta de empleo de Farmacéuticos en Dinamarca (HOVEDSTADEN)

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.

Descripción de la oferta de trabajo:
-?Research & Development -?Denmark - Måløv We are looking for an ambitious and talented person who is ready to take on the responsibility for an IT system that is essential for the logistics of our clinical trials. The job is project management oriented and independent. You must be good at interacting with many different people and be a team player. As part of Novo Nordisk’s R&D family, Chemistry, Manufacturing and Control (CMC) Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for non-clinical and clinical trials which is a complicated journey that requires about 10 years of dedicated work in CMC Development. CMC Development is an ambitious organisation with a strong culture. We always seek to solve problems, have an eye for the entire business and do our best to deliver despite any obstacles along the way. About the department Clinical Supplies is a part of CMC Development. We are responsible for the planning, production, packaging, labelling and distribution of products for Novo Nordisk clinical trials worldwide. We make sure that the required medication is provided to patients participating in our clinical trials. Our department, Clinical Supplies Project Planning (CSPP) consists of 3 teams; Project Entry, Supply Strategy and Interactive Web Response System (IWRS) (IT). The position is in the IWRS team where you will work together with 15 IWRS coordinators. The position In most of our clinical trials we use an IT-system called Interactive Web Response System (IWRS) to handle allocation of treatments to patients, manage shipments to hospitals around the world and ensure that we get the right data from our trials. The IWRS is specifically set-up for each trial, and right now we operate IWR systems for around 50 trials. It will be your responsibility to get the IWRS up and running for new trials assigned to you and to maintain it during the whole trial period. The position is a temporarily position and starts as soon as possible. Among your main tasks is to produce a specification of how the system should be programmed. The actual programming is outsourced. You will therefore need to collect input from a large number of stakeholders, in order to set-up the system so it delivers what is needed. You will also test that the system works and you will train the end-users, so there can be a few travel days per year to different countries. You will work closely with many stakeholders in Novo Nordisk worldwide e.g. international trial managers, data managers, statisticians, trial monitors, and supply chain planners as well as with our external suppliers. You will develop your skills within IT, project management, people management and management of our external supplier. You will also obtain knowledge of the drug development process. As you gather this experience you can get the opportunity to drive larger projects together with other colleagues. Qualifications There are several ways of entering this job. You can be a M.Sc. or B.Sc. within pharmaceutical science, engineering or similar, you can have a background within clinical trials (data management, trial statistician, monitors, trial management or study nurse) or your background can be within IT, preferably with clinical IT systems. We will make sure that the tasks at hand are aligned with your degree of experience and your need for development and personal challenges. We will also make sure that support from more experienced colleagues is available in your development process. We expect you to be independent, self-driven, ambitious, and good at multi-tasking and a team player who likes challenges. You must like to handle many different stakeholders and you should enjoy striving for perfection and working in a structured way. Working at Novo Nordisk At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you

Servicio de empleo de origen: AMS, Servicios Públicos de Empleo, Dinamarca.

País del trabajo: Dinamarca.

Región: Hovedstaden.

Ver 1035 ofertas de trabajo en "HOVEDSTADEN" (Dinamarca).

Fecha de inicio: 09/06/2017.

Nº de vacantes: 1.

Nivel educativo requerido: Sin especificar.

Tipo de contrato: Jornada completa.

Duración del contrato: Indefinido.

Cómo solicitar el puesto:
Mette Ellemann-Søtofte

Empresa: Novo Nordisk A/S.

Teléfono: 44448888.

Fax: 44442314.

Ver las 73 ofertas de trabajo de Profesionales científicos e intelectuales : Profesionales de la salud : Otros profesionales de la salud : Farmacéuticos ofertadas.

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