(Senior) Safety Surveillance Adviser (1 year contract)
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Søborg
Are you passionate about ensuring the safety of pharmaceutical products? Do you have experience in safety surveillance and signal detection?
We are looking for a (Senior) Safety Surveillance Adviser to join our team at Novo Nordisk in a temporary position for 1 year.
If you are ready for a new challenge and want to make a difference in the healthcare industry, read on and apply today for a life-changing career! The Position
You will get the opportunity both to work independently and in collaboration with a team of highly skilled, committed, and enthusiastic colleagues across the functional areas in , especially the Non-clinical and Clinical Development teams. Assuming responsibility, communicating information and taking action will be essential parts of your workday. Responsibilities may include:
• Establishing the product safety profile during development and maintenance of the labelling for marketed products.
• Conducting safety surveillance of products during pre-approval and post-approval phases, based on safety information from worldwide sources.
• Communicating drug safety issues internally and to health authorities as required.
• Supporting cross-functional safety committees, ensuring effective establishment and execution of meetings.
• Taking responsibility for all areas related to patient safety in clinical trials. Qualifications
To succeed in the role, we expect you to have:
• A master’s degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent). PhD/research experience, is an advantage but not a requirement.
• Experience within pharmacovigilance and or clinical development and a strong desire to specialize within safety surveillance.
• A solid understanding of medical concepts, scientific methodology, and drug development.
• Excellent communication skills, both written and spoken, with fluency in English. You are a team player who thrives in a multicultural and continuously evolving environment. At the same time, you are self-driven and capable of working independently, handling pressure, and meeting tight deadlines in a fast-paced setting. You demonstrate strong collaboration skills, effective communication, and a high degree of organization. Additionally, you are ethical, responsible, and adaptable, making you a reliable and valuable contributor to any team. About the Department
Safety Surveillance is a department within Global Patient Safety and is situated in Søborg, Denmark. We also have a department in Bangalore, India. We are globally accountable for surveillance of all safety information for ’s products that are currently marketed or under development. We additionally handle safety label updates, preparation of Risk Management Plans and aggregate reports. We treasure a positive and inclusive atmosphere in our team(s) and count on you to engage and participate in a positive manner as well. Working at
At , we don’t wait for change. We drive it. We’re 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’re all working to move the needle on patient care. Contact
For further information, please contact Senior Director Brian Sonne Stage at Deadline 7 March 2025 Applications will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible.
Please include a few sentences about why you are applying for the position in your resume or CV. You do not need to attach a cover letter to your application. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. We are looking for several Safety profiles at . Therefore, hiring managers from different teams might also look at your application. Please indicate in your application if we are not allowed to share your application.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At 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.
We are looking for a (Senior) Safety Surveillance Adviser to join our team at Novo Nordisk in a temporary position for 1 year.
If you are ready for a new challenge and want to make a difference in the healthcare industry, read on and apply today for a life-changing career! The Position
You will get the opportunity both to work independently and in collaboration with a team of highly skilled, committed, and enthusiastic colleagues across the functional areas in , especially the Non-clinical and Clinical Development teams. Assuming responsibility, communicating information and taking action will be essential parts of your workday. Responsibilities may include:
• Establishing the product safety profile during development and maintenance of the labelling for marketed products.
• Conducting safety surveillance of products during pre-approval and post-approval phases, based on safety information from worldwide sources.
• Communicating drug safety issues internally and to health authorities as required.
• Supporting cross-functional safety committees, ensuring effective establishment and execution of meetings.
• Taking responsibility for all areas related to patient safety in clinical trials. Qualifications
To succeed in the role, we expect you to have:
• A master’s degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent). PhD/research experience, is an advantage but not a requirement.
• Experience within pharmacovigilance and or clinical development and a strong desire to specialize within safety surveillance.
• A solid understanding of medical concepts, scientific methodology, and drug development.
• Excellent communication skills, both written and spoken, with fluency in English. You are a team player who thrives in a multicultural and continuously evolving environment. At the same time, you are self-driven and capable of working independently, handling pressure, and meeting tight deadlines in a fast-paced setting. You demonstrate strong collaboration skills, effective communication, and a high degree of organization. Additionally, you are ethical, responsible, and adaptable, making you a reliable and valuable contributor to any team. About the Department
Safety Surveillance is a department within Global Patient Safety and is situated in Søborg, Denmark. We also have a department in Bangalore, India. We are globally accountable for surveillance of all safety information for ’s products that are currently marketed or under development. We additionally handle safety label updates, preparation of Risk Management Plans and aggregate reports. We treasure a positive and inclusive atmosphere in our team(s) and count on you to engage and participate in a positive manner as well. Working at
At , we don’t wait for change. We drive it. We’re 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’re all working to move the needle on patient care. Contact
For further information, please contact Senior Director Brian Sonne Stage at Deadline 7 March 2025 Applications will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible.
Please include a few sentences about why you are applying for the position in your resume or CV. You do not need to attach a cover letter to your application. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. We are looking for several Safety profiles at . Therefore, hiring managers from different teams might also look at your application. Please indicate in your application if we are not allowed to share your application.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At 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 21.2.2025, 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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