Novo Nordisk A/S
Gladsaxe, 1 stilling
- Pharmacovigilance
- Denmark - Bagsværd
We are looking for a Senior Clinical Safety Associate to join the Safety Operations (SO) Case Management II team in a permanent position.
About the department
The SO Case Management II team is part of the Safety Operations Case Management Department in Safety Operations and is thereby 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 team consists of 12 highly engaged colleagues; we are working in a fast-paced environment reflecting the increasing demands from regulatory authorities. Geographically the department is situated in Bagsværd.
The position
As a Senior Clinical Safety Associate you will be responsible for handling adverse events reported world-wide from Novo Nordisk A/S clinical trials to ensure that global regulatory requirements are met. You should use your medical skills to evaluate individual case stories and it is expected that you can provide guidance to colleagues and relevant stakeholders in all case handling aspects.
As a Senior Clinical Safety Associate you should be able to foresee which impact, changes to case handling related processes will have on other interlinked and related processes. The job may involve participation in projects in Global Safety, or in other parts of the organisation, in addition to being responsible for preparing SOPs/working instructions where it is expected that you can act independently as Subject Matter Expert within the case handling field. Deadlines, cross-functional collaboration, and international communication will be part of your workday.
Qualifications
You have an educational background as a nurse and minimum 3 years of experience within the pharmacovigilance and case handling field. You have in depth knowledge of all case handling processes and are able to explain case handling processes with reference to relevant SOPs, working instructions and regulatory requirements. You are proficient within both written and spoken English. You have flair for using IT systems and you are highly skilled within MS Office, including Excel. As a person you are self-driven, have excellent learning- and analytical skills with a strong ability to communicate, plan and coordinate multiple simultaneous activities. You promote knowledge sharing and focus on ‘win-win’ solutions. You are diligent, show flexibility and are a good team player.
We offer an exciting job with lots of challenges among good colleagues in a positive working environment. The application should be written in English.
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, please contact Lotte Finderup +45 3079 5078.
Deadline
29 March 2016.
