stillingsbetegnelse: Event Adjudication Adviser

jobbeskrivelse:
- Pharmacovigilance - Denmark - Bagsværd Are you interested in pharmacovigilance and clinical trials? Do you want to cooperate with stakeholders across the organisation? Then we may have the right job for you. We are looking for an Event Adjudication Adviser to join our Safety Operations (SO) Event Adjudication department. About the department The Event Adjudication Adviser department belongs to Safety Operations, one of the functional areas in Global Safety. Global Safety is responsible for the global handling and reporting of adverse events to authorities, and the surveillance of the safety and quality of Novo Nordisk clinical development and marketed products. The department is situated in Bagsværd. The Event Adjudication adviser department consists of 22 highly engaged team members from various academic backgrounds; who work in a fast-paced environment reflecting increasing demands from numerous long term clinical trials and regulatory authority requirements. In an increasing number of trials, certain clinical adverse events are required to be adjudicated. Event adjudication is a process where an independent review board of medical specialists assesses the relevant events for fulfilment of pre-defined clinical criteria. The job As an Event Adjudication Adviser you will be a driving factor between Safety Operations, Data Management, Global Development and external service providers dealing with event adjudication in selected projects. You will make the first assessment of the events and ensure that all documentation is made timely available for the final event adjudication. Project management, process setup, on-going event tracking, documentation review, and creating and communicating reports are examples of what this dynamic role comprises of. The role varies according to the life of a clinical trial with regard to pace and task type. Some of these tasks are data and database driven. The job will require some travel. Qualifications You hold a university degree in medical, biological, pharmaceutical science (e.g. Medicine, Pharmacy, Veterinary) or related disciplines. Experience in pharmacovigilance, event adjudication, Good Clinical Practice (GCP) and/or project management is an advantage. The job requires proficiency in English, in addition to high communication-, coordination and planning capacities and a strong quality mind-set. You are proficient in the Microsoft Office Package. You are proactive and like to work independently, as well as in a team. You have excellent cooperative skills and a high degree of flexibility. As a person you are open-minded, dynamic, and eager to learn new processes and have a positive attitude to challenges. 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 about the job please contact Ane Skou Elgaard +45 3075 0958. Deadline 11 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