stillingsbetegnelse: Trial Allocation Consultant

jobbeskrivelse:
- Research & Development - Denmark - Søborg Allocation of patients to clinical trials and countries within Novo Nordisk is handled by Global Trial Allocation (GTA). We work with this responsibility in a global and complex environment interacting with many stakeholders across the CMR organisation and Global Development projects in HQ. Novo Nordisk will in the coming years have an increasingly high activity level within clinical trials and product approvals. Hence transparency around the country allocations supported by in depth analysis and risk mitigations is key for a successful trial execution. About the department GTA is anchored in Strategic Development within Global Development, with the purpose of allocating patients into clinical trials incorporating all relevant parameters for the specific trial while ensuring patient commitment is anchored in the CMR organisation. The department consists of four dedicated employees each with responsibilities towards the CMR organisation and Global Development projects. The job You will be responsible (project lead) for the global patient allocation into a number of clinical trials. Patient allocation is based on a combined quantitative and qualitative approach, where clinical trial characteristics together with different and varied datasets are considered. Your overall task will be to translate this information, and combine it with cross-portfolio strategic considerations and insights into the CMR organisation, reaching meaningful and operational trial allocations. The day to day activities of the department will bring you in close contact with the Global Development projects, and the CMR organisation. The GTA function has become a natural centre of excellence within short term patient forecasting, analysis, and strategic evaluations and we interact with many stakeholders globally and cross-functionally. You will report to the Director of GTA and as part of Strategic Development, Global Development, and you will work closely with colleagues within this area. Qualifications You have a relevant University degree and analytical background. You could have a Bachelor or M.Sc. in natural science (eg. medicine, pharmacy, biology) with strong analytical skills and strong communication skills. You may also have experience from clinical trial execution. You must be analytical, quality conscious, and have a track record within conduct of complex, cross-functional projects. In addition you have advanced Microsoft Excel and PowerPoint skills. As you will be working closely with colleagues across the organisation, it is very important that you have strong communication and stakeholder management skills. You are good at ‘talking with data and insights’. You have pharmaceutical industry experience, and proven experience working within e.g. clinical operations. You are fluent in English, written and speech. An understanding and/or knowledge of clinical development within Novo Nordisk will be an advantage. 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 Henrik Troelsen at mobile +45 3079 4507. Deadline 22 October 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