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Do you have a passion about Clinical Trials? Do you eager to learn about pharmaceutical products and setting up clinical trials? Do you want to make a difference and contribute to the well-being of people all over the world? If yes, then we have the perfect opportunity for you!
As part of Novo Nordisk’s R&ED family, CMC Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for all Novo Nordisk non-clinical and clinical trials.
The position
You will join a team of dedicated professionals responsible for setting up, planning and coordinating clinical supplies for trials execution in Novo Nordisk. This includes ensuring relevant input from a clinical supply perspective to clinical protocol, taking relevant input from the clinical trial protocol and product documents making it into trial master data, ensuring clinical labels texts are aligned with product specifications and regulatory requirements and trial specific manuals to be used by clinical sites. In this role you will be responsible for both planning and conducting activities to ensure documents are ready for clinical trial application to authorities and for planning of clinical trial product ready for patients participating in clinical trials.
Together with experienced colleagues, you will be involved in developing processes in our team that will enable us to work smarter in an informal working environment with a high degree of empowerment. To succeed in the job, you will establish and maintain ongoing collaboration with a wide range of stakeholders within different areas in Novo Nordisk.
Qualifications
You hold a bachelor’s or Master’s degree within Engineering, Pharmaceutical science or similar. You have minimum 2 year of relevant experience from the pharmaceutical industry. The ideal candidate also have:
You work independently and structured and prioritise your tasks in an ever-changing and dynamic environment. You have a positive mind-set and strong sense of responsibility, and take pride in proactively delivering high-quality work on time.
You are a dedicated team player, who inspires trust amongst your colleagues and stakeholders and are good at establishing and maintaining stakeholder relations. You aspire to continuously learn and you take challenges as opportunities to grow.
About the department
Clinical Supplies Trial Set-up is a part of Clinical Supplies in CMC Development. In Clinical Supplies, we ensure trial products on time, in the right quality and quantity for all clinical trials conducted by Novo Nordisk
The department consist of four teams, responsible for preparing and planning execution of clinical trials by translating protocol and scientific documents and setting up the label package for clinical trial application, forecasting product demand, planning packaging of trial products and setting up the Randomisation and Trial Supply Management system
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 extraordinary talent and benefit from a range of possibilities for professional and personal development
Contact
For further information, please contact Associate Manager Laila Baadsgaard, +45 30 79 97 93
Deadline 15. November 2022
Please note that applications will be reviewed on an ongoing basis and interviews will be scheduled as soon as suitable candidates are identified.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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.
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As part of Novo Nordisk’s R&ED family, CMC Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for all Novo Nordisk non-clinical and clinical trials.
The position
You will join a team of dedicated professionals responsible for setting up, planning and coordinating clinical supplies for trials execution in Novo Nordisk. This includes ensuring relevant input from a clinical supply perspective to clinical protocol, taking relevant input from the clinical trial protocol and product documents making it into trial master data, ensuring clinical labels texts are aligned with product specifications and regulatory requirements and trial specific manuals to be used by clinical sites. In this role you will be responsible for both planning and conducting activities to ensure documents are ready for clinical trial application to authorities and for planning of clinical trial product ready for patients participating in clinical trials.
Together with experienced colleagues, you will be involved in developing processes in our team that will enable us to work smarter in an informal working environment with a high degree of empowerment. To succeed in the job, you will establish and maintain ongoing collaboration with a wide range of stakeholders within different areas in Novo Nordisk.
Qualifications
You hold a bachelor’s or Master’s degree within Engineering, Pharmaceutical science or similar. You have minimum 2 year of relevant experience from the pharmaceutical industry. The ideal candidate also have:
- a strong quality mindset and experience with regulatory requirements and GxP.
- data-driven mindset and flair for IT and is used to working with different IT systems
- good process understanding, seek simple solutions and see continuous improvement as a natural part of processes.
- strong collaboration and effective communication skills and are fluent in Danish and English.
You work independently and structured and prioritise your tasks in an ever-changing and dynamic environment. You have a positive mind-set and strong sense of responsibility, and take pride in proactively delivering high-quality work on time.
You are a dedicated team player, who inspires trust amongst your colleagues and stakeholders and are good at establishing and maintaining stakeholder relations. You aspire to continuously learn and you take challenges as opportunities to grow.
About the department
Clinical Supplies Trial Set-up is a part of Clinical Supplies in CMC Development. In Clinical Supplies, we ensure trial products on time, in the right quality and quantity for all clinical trials conducted by Novo Nordisk
The department consist of four teams, responsible for preparing and planning execution of clinical trials by translating protocol and scientific documents and setting up the label package for clinical trial application, forecasting product demand, planning packaging of trial products and setting up the Randomisation and Trial Supply Management system
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 extraordinary talent and benefit from a range of possibilities for professional and personal development
Contact
For further information, please contact Associate Manager Laila Baadsgaard, +45 30 79 97 93
Deadline 15. November 2022
Please note that applications will be reviewed on an ongoing basis and interviews will be scheduled as soon as suitable candidates are identified.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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.
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 Måløv.
Jobbet er oprettet på vores service den 2.11.2022, 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.
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