Clinical Publisher
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Søborg
Are you a fast learner and interested in clinical development and documentation? Do you have a quality mindset and a flair for learning new software? We are now looking for a Clinical Publisher for our clinical publishing team in Søborg.
The position
The position offers a unique opportunity to work with collecting, checking, and compiling relevant clinical documentation from many different stakeholders throughout the organisation. You ensure that we have all the relevant clinical documents needed for regulatory submissions and that they are delivered in the right electronic quality to Regulatory Affairs.
Your main tasks will include
Electronic quality control of documents to ensure adherence to regulatory requirements such as file size, bookmarks, links, margins etc.
Supporting, training, and coaching our clinical organisation in the use of various databases and templates to store clinical information.
Engaging in projects developing and implementing digital solutions for publishing.
Training Medical Writers, Affiliates, Trial Management, and other colleges in our publishing processes.
Ideal Candidate
Our ideal candidate holds a master’s degree- this could be within library science and have a flair for learning new systems and software. You are a fast learner and possess excellent communication skills. As a person you are both proactive and service minded. You can keep an overview while prioritising and balancing different types of tasks. Having a quality mind-set is a must and you can keep deadlines. You work independently but are also a natural team player who thrives on contributing to any team you are part of.
Qualifications
• Master’s degree in library science or similar
• Extensive and broad experience from working in either the pharmaceutical or publishing industries
• Experience in editing and preparing documentation in Excel, Word, and Adobe Acrobat Pro
• Be a fast learner with an eye for detail, and able to quickly pick up new software skills
• Be flexible and structured, and able to thrive in a fast-changing work environment while maintaining high standards of accuracy, quality, and customer service to stakeholders
• Be proactive, capable of working independently, and being able to prioritise and plan own tasks, while at the same time being an active contributor to the success and harmony of the entire team
• Be a skilled communicator who is fluent in both written and spoken English.
About the department
The position is based in the Clinical Publishing, Transparency and Archiving Department located in Søborg, Denmark, where we are a team of 16 dedicated colleagues. We share an interest in supporting our drug development projects with our specific areas of expertise.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For further information, please reach out to Morten Gadgaard at +45 3079 7487.
Deadline
5. March 2023. Candidates will be evaluated and interviewed on an ongoing basis.
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to applying for this position in your resume or CV.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
Should you wish to learn more about working at Novo Nordisk, here may be a good place for you to begin: https://www.novonordisk.com/careers/working-at-novo-nordisk.html 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.
The position
The position offers a unique opportunity to work with collecting, checking, and compiling relevant clinical documentation from many different stakeholders throughout the organisation. You ensure that we have all the relevant clinical documents needed for regulatory submissions and that they are delivered in the right electronic quality to Regulatory Affairs.
Your main tasks will include
Electronic quality control of documents to ensure adherence to regulatory requirements such as file size, bookmarks, links, margins etc.
Supporting, training, and coaching our clinical organisation in the use of various databases and templates to store clinical information.
Engaging in projects developing and implementing digital solutions for publishing.
Training Medical Writers, Affiliates, Trial Management, and other colleges in our publishing processes.
Ideal Candidate
Our ideal candidate holds a master’s degree- this could be within library science and have a flair for learning new systems and software. You are a fast learner and possess excellent communication skills. As a person you are both proactive and service minded. You can keep an overview while prioritising and balancing different types of tasks. Having a quality mind-set is a must and you can keep deadlines. You work independently but are also a natural team player who thrives on contributing to any team you are part of.
Qualifications
• Master’s degree in library science or similar
• Extensive and broad experience from working in either the pharmaceutical or publishing industries
• Experience in editing and preparing documentation in Excel, Word, and Adobe Acrobat Pro
• Be a fast learner with an eye for detail, and able to quickly pick up new software skills
• Be flexible and structured, and able to thrive in a fast-changing work environment while maintaining high standards of accuracy, quality, and customer service to stakeholders
• Be proactive, capable of working independently, and being able to prioritise and plan own tasks, while at the same time being an active contributor to the success and harmony of the entire team
• Be a skilled communicator who is fluent in both written and spoken English.
About the department
The position is based in the Clinical Publishing, Transparency and Archiving Department located in Søborg, Denmark, where we are a team of 16 dedicated colleagues. We share an interest in supporting our drug development projects with our specific areas of expertise.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For further information, please reach out to Morten Gadgaard at +45 3079 7487.
Deadline
5. March 2023. Candidates will be evaluated and interviewed on an ongoing basis.
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to applying for this position in your resume or CV.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
Should you wish to learn more about working at Novo Nordisk, here may be a good place for you to begin: https://www.novonordisk.com/careers/working-at-novo-nordisk.html 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 9.2.2023, 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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| Dato | Alle jobs som forretningsudviklere |
|---|---|
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| 20. november 2024 | 15 |
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| 31. oktober 2024 | 8 |
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| 28. oktober 2024 | 6 |
| 27. oktober 2024 | 7 |
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| 25. oktober 2024 | 8 |
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