stillingsbetegnelse: Senior Safety Surveillance Adviser

jobbeskrivelse:
- Pharmacovigilance - Denmark - Bagsværd Is drug safety important to you? Are you excited by digging into information to find answers? Do you want to play a key role in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk products? You may be our new colleague in Safety Surveillance Insulin & Devices. About the department Safety Surveillance Insulin & Devices is a department within Global Safety and is situated in Bagsværd. Our team of dedicated and skilled professionals has global responsibility for the surveillance of all safety information for Novo Nordisk’s insulin products that are currently marketed or under development. The job The position as a Senior Safety Surveillance Adviser is open for immediate placement. You will be responsible for the ongoing safety surveillance of one or more products. This responsibility includes analysis of aggregate safety data, medical evaluation of safety information, safety signal detection and medical input to safety reporting and benefit risk assessment. You may also be chairing a drug safety committee and be safety representative in cross-functional teams and will contribute to development of clinical trial protocols for drug development and clinical trial reports. Your job responsibilities may also include communication with external parties related to clinical safety monitoring, such as Data Monitoring Committees. You will work independently and in collaboration with a team of highly skilled, committed and enthusiastic colleagues. Assuming responsibility, communicating information and taking action will be essential parts of your work day. You will have a close collaboration and interaction with other functional areas in Novo Nordisk, especially the clinical development team and regulatory affairs team. Qualifications You have a medical doctor (MD) degree or a university degree within Natural Sciences (DVM, M.Sc. Pharm. or equivalent) and solid experience with pharmacovigilance as well as analysing and interpreting large datasets and making conclusions based on data. A good understanding of medical concepts, disease processes, scientific methodology, drug development and data analysis is important and experience within drug development is an advantage. As a person you are responsible, well-organised, a self-starter, able to work under pressure when needed, have a strong analytical sense and are curious. You are a team player, and you are good at establishing contact and collaborating with stakeholders. You must be fluent in English, both written and spoken and be an experienced user of MS Office (Excel, PowerPoint, Word, and Outlook). 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 Ona Kinduryte at +45 3079 8308 or Poul-Martin Haahr at +45 3075 4082. Deadline 25 September 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