Temporary Senior Scientist
- Research & Development
- Denmark - Måløv
Do you want to be part of our dynamic toxicologist group at Novo Nordisk?
A temporary toxicologist position (Senior Scientist) is open for employment in the Department of Toxicology and Safety Pharmacology Diabetes, in Måløv from 1st of March 2014 to 28th of February 2015.
About the department
The department is overall responsible for performing non-clinical studies supporting the safety assessment of drug candidates throughout development. Furthermore, we also provide toxicological support to material characterization in device projects and toxicological assessments to Product Supply. Our department is characterized by an open, innovative and ambitious atmosphere with good opportunities for further development of the employees.
The Job
You will be allocated to drug development projects, where you will be representing the scientific area of our department. This includes coordination of activities with a variety of internal and external stakeholders. The focus for your projects will lie within our diabetes portfolio and your role will be to plan, secure performance of, and report state of the art non-clinical in vivo and in vitro safety studies. You will be integrating data from these studies and other sources and thereby support a safety assessment of our drug candidates. You will be responsible for the scientific quality of reports and other documentation for submission to regulatory authorities in accordance with international guidelines. Occasionally, you may be responsible for safety evaluations of inactive ingredients.
Qualifications
You have a science degree combining solid understanding of physiology and disease. You have experience in experimental work and preferably an educational or professional background in toxicology. Ideally you have experience with drug development of pharmaceutical drug candidates including involvement in the non-clinical safety assessment of biopharmaceuticals. We will take care of any necessary additional training, coaching and education. We expect that you are clear in your communication, possess excellent written and spoken English skills and focus on providing high-quality, timely results in close collaboration with your colleagues in the project team
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.
Contact
For further information, please contact Ingrid Brück Bøgh at +45 3075 4515.
Deadline
3 January 2014
- Research & Development
- Denmark - Måløv
Do you want to be part of our dynamic toxicologist group at Novo Nordisk?
A temporary toxicologist position (Senior Scientist) is open for employment in the Department of Toxicology and Safety Pharmacology Diabetes, in Måløv from 1st of March 2014 to 28th of February 2015.
About the department
The department is overall responsible for performing non-clinical studies supporting the safety assessment of drug candidates throughout development. Furthermore, we also provide toxicological support to material characterization in device projects and toxicological assessments to Product Supply. Our department is characterized by an open, innovative and ambitious atmosphere with good opportunities for further development of the employees.
The Job
You will be allocated to drug development projects, where you will be representing the scientific area of our department. This includes coordination of activities with a variety of internal and external stakeholders. The focus for your projects will lie within our diabetes portfolio and your role will be to plan, secure performance of, and report state of the art non-clinical in vivo and in vitro safety studies. You will be integrating data from these studies and other sources and thereby support a safety assessment of our drug candidates. You will be responsible for the scientific quality of reports and other documentation for submission to regulatory authorities in accordance with international guidelines. Occasionally, you may be responsible for safety evaluations of inactive ingredients.
Qualifications
You have a science degree combining solid understanding of physiology and disease. You have experience in experimental work and preferably an educational or professional background in toxicology. Ideally you have experience with drug development of pharmaceutical drug candidates including involvement in the non-clinical safety assessment of biopharmaceuticals. We will take care of any necessary additional training, coaching and education. We expect that you are clear in your communication, possess excellent written and spoken English skills and focus on providing high-quality, timely results in close collaboration with your colleagues in the project team
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.
Contact
For further information, please contact Ingrid Brück Bøgh at +45 3075 4515.
Deadline
3 January 2014