Safety Surveillance Adviser
- Research & Development, Medical Doctor
- Denmark - Gentofte
Are you a rheumatologist or an expert in drug safety within the area of autoimmune and chronic inflammatory diseases? If yes, you may be our new colleague in Safety Surveillance Biopharm. We are seeking an experienced colleague, who is prepared to play a key role in patient safety.
About the department
We are an international team of 6 medical doctors/scientists. Safety Surveillance Biopharm has the global responsibility for the ongoing evaluation and management of the safety profile for products belonging to the product portfolio in development for autoimmune and chronic inflammatory diseases, as well as marketed products such as Growth Hormone therapy, Hormone Replacement Therapy in postmenopausal women and oral anti-diabetic treatment.
The job
Your key responsibility resides within the product portfolio in clinical development for autoimmune and chronic inflammatory diseases. This includes evaluation and management of safety data, signal detection, periodic safety update reporting, development of patient safety information and risk management activities.
You will resume the role as chairperson for a product specific cross functional safety committee, which is the authority within Novo Nordisk responsible for providing integrated assessments of safety data and endorsing appropriate actions for the product in question.
Cross-functional collaboration, in particular with global development and regulatory affairs, in a multicultural, international environment will be part of your workday.
You will work in a fast-paced environment reflecting the increasing demands from regulatory authorities while always bearing patient safety in mind.
Qualifications
You have a medical degree or equally relevant science degree topped with solid experience in one or more of the following disciplines: drug safety, pharmacovigilance, clinical development or pharmaco-epidemiology. Clinical or drug safety experience within the field of rheumatology, autoimmune or chronic inflammatory diseases is an advantage.
You are enthusiastic, energetic, confident and a strong team player. Evidently, you have a good sense of urgency and are able to cope well under pressure still maintaining a good sense of humour. You have demonstrated planning as well as analytical skills.
You are fluent in both written and spoken English, experienced user of the Microsoft Office package and possess strong communication and presentation skills.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please contact Birgitte Scharling at +45 3075 5292 or Hanne Rasmussen at +45 3079 7450.
Deadline
17 June 2013.
- Research & Development, Medical Doctor
- Denmark - Gentofte
Are you a rheumatologist or an expert in drug safety within the area of autoimmune and chronic inflammatory diseases? If yes, you may be our new colleague in Safety Surveillance Biopharm. We are seeking an experienced colleague, who is prepared to play a key role in patient safety.
About the department
We are an international team of 6 medical doctors/scientists. Safety Surveillance Biopharm has the global responsibility for the ongoing evaluation and management of the safety profile for products belonging to the product portfolio in development for autoimmune and chronic inflammatory diseases, as well as marketed products such as Growth Hormone therapy, Hormone Replacement Therapy in postmenopausal women and oral anti-diabetic treatment.
The job
Your key responsibility resides within the product portfolio in clinical development for autoimmune and chronic inflammatory diseases. This includes evaluation and management of safety data, signal detection, periodic safety update reporting, development of patient safety information and risk management activities.
You will resume the role as chairperson for a product specific cross functional safety committee, which is the authority within Novo Nordisk responsible for providing integrated assessments of safety data and endorsing appropriate actions for the product in question.
Cross-functional collaboration, in particular with global development and regulatory affairs, in a multicultural, international environment will be part of your workday.
You will work in a fast-paced environment reflecting the increasing demands from regulatory authorities while always bearing patient safety in mind.
Qualifications
You have a medical degree or equally relevant science degree topped with solid experience in one or more of the following disciplines: drug safety, pharmacovigilance, clinical development or pharmaco-epidemiology. Clinical or drug safety experience within the field of rheumatology, autoimmune or chronic inflammatory diseases is an advantage.
You are enthusiastic, energetic, confident and a strong team player. Evidently, you have a good sense of urgency and are able to cope well under pressure still maintaining a good sense of humour. You have demonstrated planning as well as analytical skills.
You are fluent in both written and spoken English, experienced user of the Microsoft Office package and possess strong communication and presentation skills.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please contact Birgitte Scharling at +45 3075 5292 or Hanne Rasmussen at +45 3079 7450.
Deadline
17 June 2013.