Safety Sytem Professional

Working area

Computing, engineering, science professionals
   Computing professionals
        Computer systems designers and analysts

JOB DESCRIPTION:

- Pharmacovigilance - Denmark - Bagsværd We are looking for a Safety System Professional to join our Safety Operations (SO) Maintenance & Support department in a permanent position in DK starting 01-NOV-2015. About the department SO Maintenance & Support is one of the functional teams in Safety Operations within Global Safety. Global Safety is globally responsible for handling adverse events, monitoring product safety, customer complaints and potential recalls in Novo Nordisk. As a Safety System Professional, you will be working across departments and functions in Global Safety and liaise with external stakeholders including Corporate IT, Global Development and Regulatory Affairs. You will be part of a team of 14 highly engaged colleagues with different professional background responsible for operating and maintaining the global safety database Argus and reporting individual case safety reports to regulatory authorities globally. The job Your main responsibility is to ensure development and continuous improvement of the global safety database Argus. this include configuring safety data in compliance with internal data standards and supporting implementation of new procedures based on increased regulatory requirements or in accordance with Global Safety´s strategic framework. You will likewise be participating in projects including IT projects and business improvement projects across the organisation where your role will be expected to provide subject matter expert input, perform informal and formal business testing and to ensure that new requirements are communicated to relevant Global Safety areas and anchored in processes and procedures as applicable. Together with your colleagues you will also be supporting end-users in business critical systems within the area. This entails front-end trouble shooting, incident reporting and identification of improvement initiatives. Qualifications You have a university degree in a biomedical or computer science discipline and experience working with relational databases, preferably Argus or Aris Global. Experience with pharmacovigilance and SQL is an advantage. The desired candidate has a structured approach to tasks, show commitment, initiative and flexibility and has a good sense of humour. You are open-minded and enthusiastic, a strong team player who can take responsibility and finalise assigned tasks. The role requires strong analytical skills including the ability to focus on details and adherence to standards while maintaining a balanced business perspective. Independent and self-promoted initiatives are required to assess the impact of new regulations within pharmacovigilance. You are fluent in written and spoken English on a professional level and feel comfortable working with colleagues from different cultural backgrounds. The application should be written in English. 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 Sascha Honig +45 3075 1266. Deadline 20 September 2015.

Work hours:

• Without entering work hours
  

Requirements

source: https://www.ec.europa.eu/eures

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