Arbejde Event Adjudication Professional in Global Safety unspecified NOVO NORDISK A/S - jobtilbud

GÆLDER
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reference: 4869909

documentId: 4869909

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lastModificationDate: 1535436185963

stillingsbetegnelse: Event Adjudication Professional in Global Safety

jobbeskrivelse:

Are you knowledgeable within drug development and has robust experience with clinical trial conduct and operational project management? 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 Professional for a maternity cover to join our Safety Operations (SO) Event Adjudication department (The cover is planned to end on 31 August 2019).

About the department
The Event Adjudication department consists of 20 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 Event Adjudication department belongs to Safety Operations, one of the functional areas in Global Safety and the department is situated in Bagsværd. 

The position
As an Event Adjudication Professional you will be a driving factor between Safety Operations, different stakeholders in Global Development e.g. Medical & Science, Data Management & Trial Management and external service providers (CROs) dealing with event adjudication in selected clinical development projects. You will be involved in setting up and ensuring processes for event adjudication on clinical trials in close cooperation with the internal and external stakeholders. Project management, CRO oversight, on-going event tracking, process document preparation, 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. Knowledge of clinical development methodology is a prerequisite and experience in event adjudication, pharmacovigilance, Good Clinical Practice (GCP) and 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 highly skilled 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.

We offer an exciting job with lots of challenges among good colleagues in a positive working environment.

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 about the job please contact Ane Skou Elgaard at +45 3075 0958 or Kirsten Bang Rungby at +45 3079 6242.

Deadline
10 September 2018.

Please notice that the applications will be evaluated as they come in.



numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2421

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positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: NOVO NORDISK A/S

source: DK-STAR

GÆLDER

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