Neurologist for Safety Surveillance, Global Safety
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Søborg
Are you a neurologist or a medical doctor with extensive experience in the neurological field: would you like to work in a global setting and 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 this is your unique opportunity to be our new colleague in Safety Surveillance. About Safety Surveillance
Safety Surveillance is a department within Global Safety, situated in Søborg, Denmark. We are globally responsible for surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development. 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. The Position
We are looking for an experienced neurologist, who can support the ongoing safety surveillance of products in clinical development stage II & III as well as for marketed products. You will drive clinical, medical and scientific expertise in relation to important neurological safety issues identified across the Safety Surveillance function. You will give valuable input and drive discussions that fall within the neurological field. Your responsibilities will also include: • Ensure medically sound input to regulatory interactions
• With focus on the neurological part, perform critical analysis and medical evaluation of the emerging aggregate safety data and contribute to establishment of the product safety profile during development and post-marketing stages
• Contribute to development of clinical trial protocols and clinical trial reports by using your neurological expertise on collection and assessment of safety information
• Represent Safety Surveillance in cross-functional teams, as relevant
• 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 especially the Non-clinical, Clinical Development and Regulatory Affairs team and it will give you an extensive insight to the whole Novo Nordisk value-chain. Qualifications
You are a MD with a proven clinical and scientific background (doctoral thesis, PhD, or publications) in neurology. You preferably have
• Prior experience within pharmacovigilance from the pharmaceutical industry
or
• Experience from clinical development within the pharmaceutical industry and strong urge to specialise within pharmacovigilance. As a person you are ethical, responsible, well-organised and a strong communicator. You thrive in a fast-paced environment in continuous development, and you are good at establishing contact, collaborating and communicating with stakeholders. You are a strong driver and a dedicated team player who enjoys a multicultural environment of continuous development. You are fluent in English (company language) both written and spoken and an experienced user of MS Office. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive change. 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, stiving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further. Together, we’re life changing. Contact
For further information on the role, please contact Cecilie Freddie Lange at +45 3079 4908. Deadline
15th June 2023. Applications will be evaluated in an ongoing process and candidates may be called for interview before the deadline. You do not need to attach a cover letter to your application, but please submit an English version of your resume and include a few sentences about your motivation towards this position.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your 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.
Safety Surveillance is a department within Global Safety, situated in Søborg, Denmark. We are globally responsible for surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development. 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. The Position
We are looking for an experienced neurologist, who can support the ongoing safety surveillance of products in clinical development stage II & III as well as for marketed products. You will drive clinical, medical and scientific expertise in relation to important neurological safety issues identified across the Safety Surveillance function. You will give valuable input and drive discussions that fall within the neurological field. Your responsibilities will also include: • Ensure medically sound input to regulatory interactions
• With focus on the neurological part, perform critical analysis and medical evaluation of the emerging aggregate safety data and contribute to establishment of the product safety profile during development and post-marketing stages
• Contribute to development of clinical trial protocols and clinical trial reports by using your neurological expertise on collection and assessment of safety information
• Represent Safety Surveillance in cross-functional teams, as relevant
• 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 especially the Non-clinical, Clinical Development and Regulatory Affairs team and it will give you an extensive insight to the whole Novo Nordisk value-chain. Qualifications
You are a MD with a proven clinical and scientific background (doctoral thesis, PhD, or publications) in neurology. You preferably have
• Prior experience within pharmacovigilance from the pharmaceutical industry
or
• Experience from clinical development within the pharmaceutical industry and strong urge to specialise within pharmacovigilance. As a person you are ethical, responsible, well-organised and a strong communicator. You thrive in a fast-paced environment in continuous development, and you are good at establishing contact, collaborating and communicating with stakeholders. You are a strong driver and a dedicated team player who enjoys a multicultural environment of continuous development. You are fluent in English (company language) both written and spoken and an experienced user of MS Office. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive change. 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, stiving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further. Together, we’re life changing. Contact
For further information on the role, please contact Cecilie Freddie Lange at +45 3079 4908. Deadline
15th June 2023. Applications will be evaluated in an ongoing process and candidates may be called for interview before the deadline. You do not need to attach a cover letter to your application, but please submit an English version of your resume and include a few sentences about your motivation towards this position.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your 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.
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 12.5.2023, 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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