Safety Surveillance Specialist
- Quality
- Denmark - Bagsværd
Are you a medical doctor who is passionate about patient safety? Then you may be one of our new safety surveillance specialists.
We are seeking medical doctors (MD) with documented clinical and scientific knowledge about diabetes, metabolic conditions or cardiology for two (2) full time positions as Safety Surveillance Specialist in Safety Surveillance Diabetes Insulin & Devices department of Global Safety, in Novo Nordisk A/S.
Drug safety is an integral part of drug development and is now in focus more than ever. In this job, millions of people with diabetes worldwide depend on your medical evaluation of the benefit/risk profile of the Novo Nordisk insulin products.
About the department
Safety Surveillance Diabetes Insulin & Devices is an international department of highly committed and skilled professionals with medical or pharmaceutical background. We have the global responsibility for the safety surveillance of the Novo Nordisk insulin products and devices, marketed or in clinical development.
The job
Your key responsibility will be the ongoing safety surveillance of insulin products. This includes evaluation of the safety data, early detection of safety signals and aggregate reporting hereof, as required by the EU and US legislation. Close collaboration and communication with other functional areas in Novo Nordisk, especially the clinical development team and regulatory affairs team is required.
Your job responsibilities will also include communication with external parties related to clinical safety monitoring, such as Data Monitoring Committees and Event Adjudication Committees.
Qualifications
You have a medical degree (MD) and preferable also scientific training (PhD or equivalent). It will be an advantage if you have previous experience from the pharmaceutical industry, especially from a medical department or a drug safety department. Experience from interactions with regulatory authorities will be a plus. You are a reliable, open-minded and dedicated team player, who thrives in a global environment of continuous development, and focuses on quality of work and the results of the team. Interaction with internal and external experts require proficiency in English, excellent communication, coordination and planning skills.
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Applications must be written in English.
Contact
For further information, please contact Liliana Hansen at +45 3075 0964.
Deadline
10 June 2013.
- Quality
- Denmark - Bagsværd
Are you a medical doctor who is passionate about patient safety? Then you may be one of our new safety surveillance specialists.
We are seeking medical doctors (MD) with documented clinical and scientific knowledge about diabetes, metabolic conditions or cardiology for two (2) full time positions as Safety Surveillance Specialist in Safety Surveillance Diabetes Insulin & Devices department of Global Safety, in Novo Nordisk A/S.
Drug safety is an integral part of drug development and is now in focus more than ever. In this job, millions of people with diabetes worldwide depend on your medical evaluation of the benefit/risk profile of the Novo Nordisk insulin products.
About the department
Safety Surveillance Diabetes Insulin & Devices is an international department of highly committed and skilled professionals with medical or pharmaceutical background. We have the global responsibility for the safety surveillance of the Novo Nordisk insulin products and devices, marketed or in clinical development.
The job
Your key responsibility will be the ongoing safety surveillance of insulin products. This includes evaluation of the safety data, early detection of safety signals and aggregate reporting hereof, as required by the EU and US legislation. Close collaboration and communication with other functional areas in Novo Nordisk, especially the clinical development team and regulatory affairs team is required.
Your job responsibilities will also include communication with external parties related to clinical safety monitoring, such as Data Monitoring Committees and Event Adjudication Committees.
Qualifications
You have a medical degree (MD) and preferable also scientific training (PhD or equivalent). It will be an advantage if you have previous experience from the pharmaceutical industry, especially from a medical department or a drug safety department. Experience from interactions with regulatory authorities will be a plus. You are a reliable, open-minded and dedicated team player, who thrives in a global environment of continuous development, and focuses on quality of work and the results of the team. Interaction with internal and external experts require proficiency in English, excellent communication, coordination and planning skills.
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Applications must be written in English.
Contact
For further information, please contact Liliana Hansen at +45 3075 0964.
Deadline
10 June 2013.