Safety Surveillance Specialist
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Søborg
Do you want to play a key role in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk products? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark? Then you might be our new colleague in Safety Surveillance.
The Position
As a Safety Surveillance specialist, you will together with other colleagues be responsible for the ongoing safety surveillance of oral semaglutide, which includes products in clinical development as well as marketed products.
Key responsibilities include:
You will get the opportunity to work both independently and in collaboration with a team of highly skilled, committed, and enthusiastic colleagues. Assuming responsibility, communicating information and taking action will be essential parts of your workday.
You will have a close collaboration and interaction with other functional areas in Novo Nordisk such as Clinical Development and Regulatory Affairs team and it will give you an extensive insight to the whole Novo Nordisk organisation.
Your Qualifications
As an ideal candidate, you have:
Experience with clinical development projects and/or documented scientific training (e.g. PhD) will be an advantage.
As a person you are ethical, responsible, well-organised and a strong communicator. You can work under pressure when needed. You are a strong collaborator and a dedicated team player who thrives in a multicultural environment of continuous development, and you are good at establishing contact and collaborating with stakeholders.
You are fluent in English both written and spoken (company language) and an experienced user of MS Office.
About the department
Safety Surveillance Oral Semaglutide is a department within Global Safety situated in Søborg, Denmark. Our team of dedicated and skilled professionals has global responsibility for surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. 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 Cecilie Freddie Lange +45 3079 4908
Deadline
30 November 2022
Please apply for the position no later than.
Applications will be reviewed on an ongoing basis, why you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application. To ensure an efficient and fair recruitment process, and please refrain from adding a photo in your CV but do include a few sentences about why you are applying for this position in your resume or CV.
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.
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The Position
As a Safety Surveillance specialist, you will together with other colleagues be responsible for the ongoing safety surveillance of oral semaglutide, which includes products in clinical development as well as marketed products.
Key responsibilities include:
- Perform critical analysis and medical evaluation of the emerging aggregate safety data and contribute to establishment of the product safety profile during development and early post-marketing stages
- Participate in preparation of communication about the benefit risk assessment (e.g. via Periodic Safety Update Reports, Development Safety Update Reports and Risk Management Plans)
- Contribute to development of clinical trial protocols and clinical trial reports
- Represent Safety Surveillance in cross-functional teams
- Potentially chair the internal Novo Nordisk safety committee for one or more products
You will get the opportunity to work both independently and in collaboration with a team of highly skilled, committed, and enthusiastic colleagues. Assuming responsibility, communicating information and taking action will be essential parts of your workday.
You will have a close collaboration and interaction with other functional areas in Novo Nordisk such as Clinical Development and Regulatory Affairs team and it will give you an extensive insight to the whole Novo Nordisk organisation.
Your Qualifications
As an ideal candidate, you have:
- a university degree in Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent)
- several years of experience within drug safety/pharmacovigilance or drug development
- a solid understanding of medical concepts, disease processes, scientific methodology and data analysis.
Experience with clinical development projects and/or documented scientific training (e.g. PhD) will be an advantage.
As a person you are ethical, responsible, well-organised and a strong communicator. You can work under pressure when needed. You are a strong collaborator and a dedicated team player who thrives in a multicultural environment of continuous development, and you are good at establishing contact and collaborating with stakeholders.
You are fluent in English both written and spoken (company language) and an experienced user of MS Office.
About the department
Safety Surveillance Oral Semaglutide is a department within Global Safety situated in Søborg, Denmark. Our team of dedicated and skilled professionals has global responsibility for surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. 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 Cecilie Freddie Lange +45 3079 4908
Deadline
30 November 2022
Please apply for the position no later than.
Applications will be reviewed on an ongoing basis, why you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application. To ensure an efficient and fair recruitment process, and please refrain from adding a photo in your CV but do include a few sentences about why you are applying for this position in your resume or CV.
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.
Print job Send to e-mail
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 9.11.2022, 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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