Clinical Publisher
- Research & Development
- Denmark - Søborg
Clinical Reporting is seeking a Clinical Publisher. As a Clinical Publisher you compile documentation from Novo Nordisk clinical trials and ensure it is ready for submission to regulatory authorities around the world. Experience in working with PDFs is an advantage, as are very strong English language skills and experience with and flair for IT in general.
About the department
Clinical Reporting is seated in Søborg and we are approximately 45 Medical Writers and 10 Clinical Publishers. The area comprises many different nationalities and we work together in a pleasant and informal environment.
As a Clinical Publisher you work in close collaboration with Medical Writers but you also interact with many other stakeholders throughout the global Novo Nordisk organisation.
The job
A Clinical Publisher compiles relevant clinical documentation into a Clinical Trial Report consisting of hyperlinked PDFs, ready to be part of a submission of a new drug application to regulatory authorities. As a Clinical Publisher you will learn to use novoDOCS, Novo Nordisk’s electronic document management system, and you will learn to compile and structure clinical documentation in epub, our publishing system. You will use tools such as Adobe Acrobat and ISI toolbox as part of your daily work. The job involves interaction with many different stakeholders throughout the Novo Nordisk organisation. Finally, you will be using your strong knowledge of English language, punctuation and grammar to review clinical documents for the Medical Writers.
Qualifications
You have a bachelor’s or master’s degree and have excellent English language skills, written as well as oral. It’s an advantage if you have experience in working with preparation of clinical documents targeted for regulatory submission or experience in working with PDFs in Adobe Acrobat. Applicants are expected to have solid experience with basic computer systems use (e.g. the Microsoft Office package). As a Clinical Publisher you work in a field that is regulated by Good Clinical Practice and regulatory guidelines and it is essential that you have good attention to details. The role of a Clinical Publisher is also service oriented, so a willingness to proactively share knowledge and support others is required. You work well independently but are also a team player and you can handle multiple concurrent tasks and meet challenging deadlines.
We offer an interesting and challenging job in a great team where you will experience a high degree of individual responsibility as well as good opportunities for personal development in an international atmosphere.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Kenneth Ostrowski at +45 3079 6093.
Deadline
31 July 2013.
- Research & Development
- Denmark - Søborg
Clinical Reporting is seeking a Clinical Publisher. As a Clinical Publisher you compile documentation from Novo Nordisk clinical trials and ensure it is ready for submission to regulatory authorities around the world. Experience in working with PDFs is an advantage, as are very strong English language skills and experience with and flair for IT in general.
About the department
Clinical Reporting is seated in Søborg and we are approximately 45 Medical Writers and 10 Clinical Publishers. The area comprises many different nationalities and we work together in a pleasant and informal environment.
As a Clinical Publisher you work in close collaboration with Medical Writers but you also interact with many other stakeholders throughout the global Novo Nordisk organisation.
The job
A Clinical Publisher compiles relevant clinical documentation into a Clinical Trial Report consisting of hyperlinked PDFs, ready to be part of a submission of a new drug application to regulatory authorities. As a Clinical Publisher you will learn to use novoDOCS, Novo Nordisk’s electronic document management system, and you will learn to compile and structure clinical documentation in epub, our publishing system. You will use tools such as Adobe Acrobat and ISI toolbox as part of your daily work. The job involves interaction with many different stakeholders throughout the Novo Nordisk organisation. Finally, you will be using your strong knowledge of English language, punctuation and grammar to review clinical documents for the Medical Writers.
Qualifications
You have a bachelor’s or master’s degree and have excellent English language skills, written as well as oral. It’s an advantage if you have experience in working with preparation of clinical documents targeted for regulatory submission or experience in working with PDFs in Adobe Acrobat. Applicants are expected to have solid experience with basic computer systems use (e.g. the Microsoft Office package). As a Clinical Publisher you work in a field that is regulated by Good Clinical Practice and regulatory guidelines and it is essential that you have good attention to details. The role of a Clinical Publisher is also service oriented, so a willingness to proactively share knowledge and support others is required. You work well independently but are also a team player and you can handle multiple concurrent tasks and meet challenging deadlines.
We offer an interesting and challenging job in a great team where you will experience a high degree of individual responsibility as well as good opportunities for personal development in an international atmosphere.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Kenneth Ostrowski at +45 3079 6093.
Deadline
31 July 2013.