Experienced Safety Surveillance Advisers
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Søborg
Do you want to play a key role in the safety surveillance activities in early phase development projects? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark? If so, we are looking for new experienced colleagues at Specialist and Senior Adviser level in Safety Surveillance at Novo Nordisk. Apply today for a life-changing career! The position
You will be responsible for the ongoing safety surveillance of several products in early clinical development across all therapeutic areas at Novo Nordisk. In addition, you will be performing critical analysis and medical evaluation of the emerging aggregate safety data and lead the establishment of the product safety profile during clinical development. Your other responsibilities will include:
• Chair a cross-functional drug safety committee.
• Prepare communication about the benefit risk assessment.
• Contribute to development of clinical study designs and protocols.
• Communicate with external parties related to clinical safety monitoring such as Data Monitoring Committees.
• Represent Safety Surveillance in cross-functional teams. 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 Novo Nordisk, especially the Non-clinical and Clinical Development teams. Assuming responsibility, communicating information and taking action will be essential parts of your workday. Qualifications
As an ideal candidate, you will have:
• A university degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent), preferably complemented by a PhD.
• Several years of experience within pharmacovigilance, or from early phase development within the pharmaceutical industry and a strong desire to specialise within safety surveillance.
• A solid understanding of medical concepts, disease processes, scientific methodology and drug development.
• The ability to work independently in a continuous developing environment. It is important that you are a strong collaborator who thrives in a multicultural environment of continuous development, and that you are good at establishing contacts and collaborating with stakeholders. As a person, you are self-driven and able to work independently and under pressure when needed. You are ethical, responsible, well-organised and a strong communicator. About the department
Safety Surveillance Phase I & Stem Cells is a department within Global Safety and our team of dedicated and skilled professionals has global responsibility for surveillance of safety information for all early phase development products at Novo Nordisk. Due to an increase in the number of early development projects, our department is expanding.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambitions 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 Christine Dethlefsen at +45 30751225 Deadline
7 June 2023 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 this 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 Novo Nordisk. Therefore, Hiring Managers from different teams might also look at your application.
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.
You will be responsible for the ongoing safety surveillance of several products in early clinical development across all therapeutic areas at Novo Nordisk. In addition, you will be performing critical analysis and medical evaluation of the emerging aggregate safety data and lead the establishment of the product safety profile during clinical development. Your other responsibilities will include:
• Chair a cross-functional drug safety committee.
• Prepare communication about the benefit risk assessment.
• Contribute to development of clinical study designs and protocols.
• Communicate with external parties related to clinical safety monitoring such as Data Monitoring Committees.
• Represent Safety Surveillance in cross-functional teams. 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 Novo Nordisk, especially the Non-clinical and Clinical Development teams. Assuming responsibility, communicating information and taking action will be essential parts of your workday. Qualifications
As an ideal candidate, you will have:
• A university degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent), preferably complemented by a PhD.
• Several years of experience within pharmacovigilance, or from early phase development within the pharmaceutical industry and a strong desire to specialise within safety surveillance.
• A solid understanding of medical concepts, disease processes, scientific methodology and drug development.
• The ability to work independently in a continuous developing environment. It is important that you are a strong collaborator who thrives in a multicultural environment of continuous development, and that you are good at establishing contacts and collaborating with stakeholders. As a person, you are self-driven and able to work independently and under pressure when needed. You are ethical, responsible, well-organised and a strong communicator. About the department
Safety Surveillance Phase I & Stem Cells is a department within Global Safety and our team of dedicated and skilled professionals has global responsibility for surveillance of safety information for all early phase development products at Novo Nordisk. Due to an increase in the number of early development projects, our department is expanding.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambitions 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 Christine Dethlefsen at +45 30751225 Deadline
7 June 2023 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 this 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 Novo Nordisk. Therefore, Hiring Managers from different teams might also look at your application.
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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 24.5.2023, 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.
- Forretningsudvikler
- Søborg
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