Clinical Operations Director
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Søborg
Do you have passion for leadership and want to be part of a journey into new and exciting therapeutic areas and ways of working in Clinical Operations? Are you motivated by a high level of responsibility combined with people management and global scientific collaborations? Then you might be our next colleague, read more and apply!
The position
As a Director, you will be managing a team of Clinical Project and Operations Leaders, Global Trial Managers, and Global Clinical Trial Administrators running clinical trials and usability tests in the area of device development including software as medical device (SaMD). Taking on this role is a unique opportunity to make an impact in a large and resourceful global development organisation.
Among your main responsibilities, you will be responsible for:
• Driving the global coordination of several clinical trials within one or more development programmes
• The execution of usability tests of medical device and SaMD
• The planning and allocation of the needed resources for a given trial within the clinical programme
• Management and competency development of your team members
Finally, you will lead the implementation of the Clinical Drug Development strategy, proactively ensure relevant change management activities and role model the Novo Nordisk Way.
Given that you will be working in the area of medical devices development you will deal with a different set of regulations in addition to the GCP environment.
The job is based in Soeborg, Denmark. Some travelling for meetings can be expected.
Qualifications
We are looking for a leader who can engage and inspire by setting the direction for the team while ensuring well-being and strong global collaboration.
To succeed in this role, you:
• hold a master’s or bachelor’s degree in a scientific related subject
• have several years of experience working with clinical drug development
• have previous experience with line management and project management
• have experience with operational aspects of planning and conducting global clinical trials
• are fluent in English
An interest and experience in working with Device and SaMD is considered an advantage.
You are familiar with cross-organisational and global work, and you can navigate well in a project-driven matrix organisation.
As a person, you have the ability to inspire and motivate employees to do their best while having an organised and structured approach to leading employees. Preferably you have previous successful experience in navigating well organisational transformations.
About the department
Working with trial management in the Obesity NASH and Device Clinical Operations project area, you will join a collaborative and dedicated team on a mission to create better treatments, care and innovation for patients. We cover the entire spectrum from early to late phase clinical trials in the obesity and NASH area, as well as for device delivery systems and software as a medical device for all therapeutic areas within Novo Nordisk.
This means you will work with colleagues across our affiliates, Contract Research Organizations and external partners.
Working at Novo Nordisk
At Novo Nordisk, 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 to manufacturing, marketing, and sales - we're all working to move the needle on patient care.
Contact
For further information, please contact Ulrika Qvint +45 3075 4640.
Deadline
20 January 2023
Screening and interviewing will be done on an ongoing basis so we encourage you to apply right away.
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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The position
As a Director, you will be managing a team of Clinical Project and Operations Leaders, Global Trial Managers, and Global Clinical Trial Administrators running clinical trials and usability tests in the area of device development including software as medical device (SaMD). Taking on this role is a unique opportunity to make an impact in a large and resourceful global development organisation.
Among your main responsibilities, you will be responsible for:
• Driving the global coordination of several clinical trials within one or more development programmes
• The execution of usability tests of medical device and SaMD
• The planning and allocation of the needed resources for a given trial within the clinical programme
• Management and competency development of your team members
Finally, you will lead the implementation of the Clinical Drug Development strategy, proactively ensure relevant change management activities and role model the Novo Nordisk Way.
Given that you will be working in the area of medical devices development you will deal with a different set of regulations in addition to the GCP environment.
The job is based in Soeborg, Denmark. Some travelling for meetings can be expected.
Qualifications
We are looking for a leader who can engage and inspire by setting the direction for the team while ensuring well-being and strong global collaboration.
To succeed in this role, you:
• hold a master’s or bachelor’s degree in a scientific related subject
• have several years of experience working with clinical drug development
• have previous experience with line management and project management
• have experience with operational aspects of planning and conducting global clinical trials
• are fluent in English
An interest and experience in working with Device and SaMD is considered an advantage.
You are familiar with cross-organisational and global work, and you can navigate well in a project-driven matrix organisation.
As a person, you have the ability to inspire and motivate employees to do their best while having an organised and structured approach to leading employees. Preferably you have previous successful experience in navigating well organisational transformations.
About the department
Working with trial management in the Obesity NASH and Device Clinical Operations project area, you will join a collaborative and dedicated team on a mission to create better treatments, care and innovation for patients. We cover the entire spectrum from early to late phase clinical trials in the obesity and NASH area, as well as for device delivery systems and software as a medical device for all therapeutic areas within Novo Nordisk.
This means you will work with colleagues across our affiliates, Contract Research Organizations and external partners.
Working at Novo Nordisk
At Novo Nordisk, 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 to manufacturing, marketing, and sales - we're all working to move the needle on patient care.
Contact
For further information, please contact Ulrika Qvint +45 3075 4640.
Deadline
20 January 2023
Screening and interviewing will be done on an ongoing basis so we encourage you to apply right away.
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 "Administrativ medarbejder", og befinder sig i kategorien "Kontor, handel og service".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 5.1.2023, 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.
- Administrativ medarbejder
- Søborg
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Statistik over udbudte administrative medarbejdere i Søborg over tid
| Dato | Alle jobs som administrative medarbejdere |
|---|---|
| 22. november 2024 | 5 |
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| 26. oktober 2024 | 3 |
| 25. oktober 2024 | 2 |
| 24. oktober 2024 | 2 |
| 23. oktober 2024 | 2 |