RA Professional
- Regulatory Affairs
- Denmark - Søborg
In this job you can contribute to changing possibilities in haemophilia. If you find this inspiring, and if you have keen negotiation skills and scientific insight, then we are looking for a regulatory professional to work primarily on early stage projects.
About the department
Novo Nordisk Regulatory Affairs (RA) makes medicine available to patients all over the world by ensuring rapid regulatory approval in all our markets. Regulatory Affairs is a fast-changing field, and the dedicated employees in our unit serve as Novo Nordisk’s ambassadors around the world. The RA Haemophilia area is located in the project house in Søborg. In the area, we are 35 people working with projects ranging from early to late stage development and with products already on the market.
The job
The job will involve interactions with stakeholders from the non-clinical, CMC and clinical area, and you will as such review documents from a very broad area of scientific disciplines. In Regulatory Affairs, you’ll work in a frequently changing environment where tasks and priorities may change from one day to the other. Tight deadlines, cross-departmental collaboration, project management and the challenges of international communication will be part of your workday. You’ll be expected to make an impact and to ask questions and challenge the status quo if that’s what it takes.
Qualifications
We expect you to have a university degree in science and documented professional experience working with regulatory affairs and/or drug development. As a person, you thrive in busy environments, and you bring a can-do spirit and a healthy common sense and sense of humour to your work – even when the pressure is on. You’re a strong team player, but you also enjoy working independently. You are able to read and understand regulatory legislation and guidelines and internal standard operating procedures and work accordingly. We also expect you to find new solutions to the challenges you meet. You’re organised, a good planner and a proactive problem-solver, who are able to collaborate with a lot of stakeholders. You’re also a skilled communicator who is comfortable speaking and writing in English.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth
Contact
For further information, please call Per Østergaard on +45 3075 9347 or Torben Storgaard on +45 3075 6124.
Deadline
8 September 2013.
- Regulatory Affairs
- Denmark - Søborg
In this job you can contribute to changing possibilities in haemophilia. If you find this inspiring, and if you have keen negotiation skills and scientific insight, then we are looking for a regulatory professional to work primarily on early stage projects.
About the department
Novo Nordisk Regulatory Affairs (RA) makes medicine available to patients all over the world by ensuring rapid regulatory approval in all our markets. Regulatory Affairs is a fast-changing field, and the dedicated employees in our unit serve as Novo Nordisk’s ambassadors around the world. The RA Haemophilia area is located in the project house in Søborg. In the area, we are 35 people working with projects ranging from early to late stage development and with products already on the market.
The job
The job will involve interactions with stakeholders from the non-clinical, CMC and clinical area, and you will as such review documents from a very broad area of scientific disciplines. In Regulatory Affairs, you’ll work in a frequently changing environment where tasks and priorities may change from one day to the other. Tight deadlines, cross-departmental collaboration, project management and the challenges of international communication will be part of your workday. You’ll be expected to make an impact and to ask questions and challenge the status quo if that’s what it takes.
Qualifications
We expect you to have a university degree in science and documented professional experience working with regulatory affairs and/or drug development. As a person, you thrive in busy environments, and you bring a can-do spirit and a healthy common sense and sense of humour to your work – even when the pressure is on. You’re a strong team player, but you also enjoy working independently. You are able to read and understand regulatory legislation and guidelines and internal standard operating procedures and work accordingly. We also expect you to find new solutions to the challenges you meet. You’re organised, a good planner and a proactive problem-solver, who are able to collaborate with a lot of stakeholders. You’re also a skilled communicator who is comfortable speaking and writing in English.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth
Contact
For further information, please call Per Østergaard on +45 3075 9347 or Torben Storgaard on +45 3075 6124.
Deadline
8 September 2013.