Arbejde Principal Process Development Specialist Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Principal Process Development Specialist

jobbeskrivelse:
- Biostatistics and Data Management - Denmark - Søborg Are you interested in working to improve clinical data management processes, providing training and supporting competency development in a global environment? Do you enjoy developing solutions at the process-technology interface? Do you want to be a key partner in the drug development process? Are you motivated by a challenging and rewarding workplace? Are you a strong project manager? 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 The Data Management (DM) Anchor is a group of 10 enthusiastic experts within clinical systems and data management, data management processes and standards, and quality management. The DM Anchor is responsible for developing and maintaining state-of-the-art data management processes globally and supporting data management operations with training and expert advice. We are responsible for driving a number of improvement projects across data management and clinical systems, as well participating in IT projects. We are seeking a new colleague to take up a position as Process Development Specialist, working to support and strengthen our global DM organisation. The Job The Process Development Specialist is primarily responsible for managing projects to optimise business processes and organisation, providing support and training on DM processes within and outside of DM, and facilitating knowledge sharing. You will in many cases be a project manager of smaller or bigger projects responsible for cross DM improvement involving different stakeholders. You work is primarily located in Copenhagen and you will interact stakeholders in other areas of Clinical Operations, and our outsourcing partners. Some global travelling is expected. Qualifications Most importantly, you have significant experience in the area of clinical data management with planning and conduct of DM deliverables. In addition you have documented experience or qualifications within project management. You have a master’s degree in life science, pharmaceutical science, statistical science or a similar field and you have education or experience within information management, such as computer science or programming. Knowledge of Good Clinical Practice and documented experience working in a GCP/ISO environment is essential. You have extensive experience as a presenter, and you communicate effectively in cross-cultural situations. You are capable of working independently, taking on responsibility and acting as a leader and mentor within data management and you are good at innovation. We expect you to be able to oversee several tasks in parallel without compromising the quality of your work and that you remain energetic, also when things are moving fast. Furthermore, good English skills and strong cooperation stills are necessities for the position. 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 Rikke Riisbro at +45 3079 1885. Deadline 1 June 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark

GÆLDER

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