Medical Writing Specialist
- Research & Development
- Denmark - Søborg
Clinical Reporting is looking for a medical writing specialist. You will be offered a challenging job with a significant amount of individual responsibility, and good personal development opportunities in an international and dynamic atmosphere.
About the Department
Clinical Reporting is the medical writing function at Novo Nordisk and is part of Global Development. We are currently 60+ employees, primarily medical writers and clinical publishers. We are a diverse group with different nationalities and professional backgrounds working together in a pleasant and informal atmosphere. We are responsible for preparing clinical documents for submission to regulatory authorities worldwide as well as abstracts and posters for scientific conferences and manuscripts to scientific journals.
The job
As medical writing specialist, your main tasks involve preparation of complex clinical documents within Novo Nordisk’s different therapy areas. Planning and coordination of activities in a cross-disciplinary setting is a central part of the job. Your main collaboration partners include clinicians, statisticians, regulatory affairs professionals, trial managers and data managers from Novo Nordisk headquarters and international affiliates.
Another important component of the job is mentoring and training of other medical writers, which requires the ability to provide constructive feedback. The medical writing specialist is also expected to drive sharing of better practices across projects/processes.
All documents are written in English and must comply with internal Novo Nordisk standard operating procedures as well as external guidelines.
Qualifications
You have a university degree within natural sciences (MD, M.Sc., M.Sc.Pharm. or equivalent) and ≥5 years of medical writing experience. In addition, you have a good understanding of the pharmaceutical industry, including clinical development and regulatory processes and requirements. Your professional skills also include statistics and scientific research methods, and you have experience with writing publications for scientific journals. You master written and spoken English at a professional level, and you have a flair for, and a genuine interest in scientific communication. In addition, you should be able to communicate in a reliable, professional and trustworthy manner. You are a strong team player who adapts easily to a changing environment with tight deadlines, and you are good at planning, coordinating, managing stakeholders and reaching consensus. You are thorough, structured and conscientious, and you have a good sense of humour.
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 development.
Contact
For further information, please Contact Trine Kruse on + 45 3079 6107, Lisbet Westergaard on + 45 3079 9817 or Mette Pierri Stensler-Thomsen on + 45 3075 2575
Deadline
10 January 2014
- Research & Development
- Denmark - Søborg
Clinical Reporting is looking for a medical writing specialist. You will be offered a challenging job with a significant amount of individual responsibility, and good personal development opportunities in an international and dynamic atmosphere.
About the Department
Clinical Reporting is the medical writing function at Novo Nordisk and is part of Global Development. We are currently 60+ employees, primarily medical writers and clinical publishers. We are a diverse group with different nationalities and professional backgrounds working together in a pleasant and informal atmosphere. We are responsible for preparing clinical documents for submission to regulatory authorities worldwide as well as abstracts and posters for scientific conferences and manuscripts to scientific journals.
The job
As medical writing specialist, your main tasks involve preparation of complex clinical documents within Novo Nordisk’s different therapy areas. Planning and coordination of activities in a cross-disciplinary setting is a central part of the job. Your main collaboration partners include clinicians, statisticians, regulatory affairs professionals, trial managers and data managers from Novo Nordisk headquarters and international affiliates.
Another important component of the job is mentoring and training of other medical writers, which requires the ability to provide constructive feedback. The medical writing specialist is also expected to drive sharing of better practices across projects/processes.
All documents are written in English and must comply with internal Novo Nordisk standard operating procedures as well as external guidelines.
Qualifications
You have a university degree within natural sciences (MD, M.Sc., M.Sc.Pharm. or equivalent) and ≥5 years of medical writing experience. In addition, you have a good understanding of the pharmaceutical industry, including clinical development and regulatory processes and requirements. Your professional skills also include statistics and scientific research methods, and you have experience with writing publications for scientific journals. You master written and spoken English at a professional level, and you have a flair for, and a genuine interest in scientific communication. In addition, you should be able to communicate in a reliable, professional and trustworthy manner. You are a strong team player who adapts easily to a changing environment with tight deadlines, and you are good at planning, coordinating, managing stakeholders and reaching consensus. You are thorough, structured and conscientious, and you have a good sense of humour.
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 development.
Contact
For further information, please Contact Trine Kruse on + 45 3079 6107, Lisbet Westergaard on + 45 3079 9817 or Mette Pierri Stensler-Thomsen on + 45 3075 2575
Deadline
10 January 2014