Department Managers in Safety Surveillance
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Søborg
Department Managers in Safety Surveillance
Do you want to play a key role and drive the ongoing pharmacovigilance and safety surveillance activities for Novo Nordisk products? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark, setting direction and inspiring a team of highly engaged professionals? Then you may be one of the new department managers in Safety Surveillance.We are looking for managers for our teams working within the departments of “Obesity, Liver Diseases & CagriSema” and “Diabetes and Cardiovascular disease”, respectively.About the departments
Safety Surveillance “Obesity, Liver Diseases & Cagrisema" and “Diabetes & Cardiovascular disease” are departments within Global Safety and, situated in Søborg, Denmark. We have global responsibility for the surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under clinical development in the therapeutic areas’ portfolio. This includes chairing the cross-functional safety committees, performing integrated safety evaluations and overall risk management for investigational compounds and marketed products.
With the extensive growth of Novo Nordisk’s portfolio and organisation, additional managers are needed across Safety Surveillance to ensure continued appropriate safety handling of clinical trial activities as well as proper transition to the post-marketing phase.The position
You will be responsible for leading a team currently consisting of approximately 10 dedicated safety surveillance advisors with medical and life science background.It will be your job to:
• Set direction for your team and contribute to quality improvement projects.
• Ensure safety contribution to the clinical and regulatory strategy for the respective therapeutic areas.
• Ensure the safety profile of the product(s) in your area is carefully monitored and appropriate actions taken when needed to minimise the risk for the patients.
• Supervise the internal Novo Nordisk safety committees for the product(s) your team is responsible for.
As manager of the team, you will have a close collaboration with a wide range of stakeholders from e.g. Non-clinical, Medical & Science, Regulatory Affairs and Clinical Operations. This means that building relationships with important stakeholders, and coaching and developing the people in the team is crucial for success.Qualifications
To be successful in this role you will need to have:
• A university degree within Health Sciences or Natural Sciences (MD, DVM, MSc. Pharm. or equivalent)
• A minimum 3 years of experience from the pharmaceutical industry in the medical/clinical development or pharmacovigilance departments
• A solid understanding of medical concepts, disease processes, scientific methodology and data analysis
• Ability to lead collaborative teams
• Ability to interact with many stakeholders in a continuously changing environment
Documented scientific training (e.g. PhD), experience from interactions with regulatory authorities and/or successful experience with people management will be an additional advantage. You must be fluent in English (both written and spoken) and be an experienced user of MS Office (Excel, PowerPoint, Word and Outlook).Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives. In exchange, we offer you an opportunity to work with talented co-workers and benefit from a range of possibilities for professional and personal development.
At Novo Nordisk, we do not wait for change. We drive it. We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we are all working to move the needle on patient care.Contact
For further information, please contact Peter Jelnes ([email protected]) or Charlotte G. Carson ([email protected])Deadline
Please apply for the position no later than 12 November 2023.
We will review the applications on an ongoing basis, so we encourage you to apply as soon as possible. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Do you want to play a key role and drive the ongoing pharmacovigilance and safety surveillance activities for Novo Nordisk products? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark, setting direction and inspiring a team of highly engaged professionals? Then you may be one of the new department managers in Safety Surveillance.We are looking for managers for our teams working within the departments of “Obesity, Liver Diseases & CagriSema” and “Diabetes and Cardiovascular disease”, respectively.About the departments
Safety Surveillance “Obesity, Liver Diseases & Cagrisema" and “Diabetes & Cardiovascular disease” are departments within Global Safety and, situated in Søborg, Denmark. We have global responsibility for the surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under clinical development in the therapeutic areas’ portfolio. This includes chairing the cross-functional safety committees, performing integrated safety evaluations and overall risk management for investigational compounds and marketed products.
With the extensive growth of Novo Nordisk’s portfolio and organisation, additional managers are needed across Safety Surveillance to ensure continued appropriate safety handling of clinical trial activities as well as proper transition to the post-marketing phase.The position
You will be responsible for leading a team currently consisting of approximately 10 dedicated safety surveillance advisors with medical and life science background.It will be your job to:
• Set direction for your team and contribute to quality improvement projects.
• Ensure safety contribution to the clinical and regulatory strategy for the respective therapeutic areas.
• Ensure the safety profile of the product(s) in your area is carefully monitored and appropriate actions taken when needed to minimise the risk for the patients.
• Supervise the internal Novo Nordisk safety committees for the product(s) your team is responsible for.
As manager of the team, you will have a close collaboration with a wide range of stakeholders from e.g. Non-clinical, Medical & Science, Regulatory Affairs and Clinical Operations. This means that building relationships with important stakeholders, and coaching and developing the people in the team is crucial for success.Qualifications
To be successful in this role you will need to have:
• A university degree within Health Sciences or Natural Sciences (MD, DVM, MSc. Pharm. or equivalent)
• A minimum 3 years of experience from the pharmaceutical industry in the medical/clinical development or pharmacovigilance departments
• A solid understanding of medical concepts, disease processes, scientific methodology and data analysis
• Ability to lead collaborative teams
• Ability to interact with many stakeholders in a continuously changing environment
Documented scientific training (e.g. PhD), experience from interactions with regulatory authorities and/or successful experience with people management will be an additional advantage. You must be fluent in English (both written and spoken) and be an experienced user of MS Office (Excel, PowerPoint, Word and Outlook).Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives. In exchange, we offer you an opportunity to work with talented co-workers and benefit from a range of possibilities for professional and personal development.
At Novo Nordisk, we do not wait for change. We drive it. We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we are all working to move the needle on patient care.Contact
For further information, please contact Peter Jelnes ([email protected]) or Charlotte G. Carson ([email protected])Deadline
Please apply for the position no later than 12 November 2023.
We will review the applications on an ongoing basis, so we encourage you to apply as soon as possible. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 6.11.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Apoteker
- Søborg
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