stillingsbetegnelse:
Experienced Safety Risk Manager for Clinical Trials

jobbeskrivelse:
- Engineering - Denmark - Hillerød Are you well known in all areas of safety risk management for clinical drug trials? Do you know how to coordinate device documentation and conduct safety risk analysis for devices for clinical drug trails? If this is you then we have an exciting job for you! About the department Device R&D is an area within our Global R&D organisation. We are responsible for the development of medical devices for self-treatment supporting all business areas of Novo Nordisk. Device R&D has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. To learn more about Device R&D, please visit link: http://www.novonordisk.com/device-rd You will join an international development team of highly skilled system and test engineers. You will become a member of the systems engineering support team, supporting the device innovation and ongoing development projects. The position Your task consists of two major parts: to coordinate the device documentation work, on the one hand and to conduct the safety risk analyses for the devices used in clinical drug trials, on the other hand. Being the representative of the devices used, you will coordinate among several independently working drug trials. This is not limited to organising and conducting meetings and workshops with members of various areas in Novo Nordisk, demonstrating device use for project members and preparing risk summary documentation for regulatory purposes. You will be given a broad range of responsibilities and experience a variety of tasks, working with stakeholders at all levels. The job will enhance your professional and personal development, providing you with an opportunity to further develop your skills within specialist expertise and project management. Qualifications You hold an academic degree within engineering with at least three years of experience within risk management and systems engineering preferably from the pharmaceutical or a comparable industry where quality, safety and regulatory compliance are vital to succeed. On a personal level you are self-motivated, ambitious, and result-oriented. You are good at collaborating in teams as well as with stakeholders at all levels. You have the ability to work independently and focused, working toward the desired quality and deadline making the crucial decision when necessary. In order to drive the safety risk coordination, you have both good coordination and facilitation skills, and an ability to analyse and understand complex structures and systems. Proficiency in oral and written English is essential. 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 Martin Paulsen on +45 3079 1095. Deadline 26 June 2016.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse:
Andet ingeniørarbejde (undtagen elektroteknologi)

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark