Safety Medical Writer
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Bagsværd
- Clinical Development and Medical
- Bagsværd
Are you looking for an opportunity to work in drug safety and use your skills as a scientific communicator? Do you build strong relationships with stakeholders and enjoy putting plans into action? Join us as a Safety Medical Writer and use your skills to ensure patient safety and best practice.
About the department
Safety Medical Writing is a department within Global Safety, and is situated in Bagsværd, Denmark and Bangalore, India. Global Safety is an organisation of more than 400 highly professional people with a high level of education within natural science. Safety Medical Writing is responsible for reporting on the emerging safety based on routine surveillance of all Novo Nordisk’s products (both currently marketed and under development worldwide), to ensure patient safety.
The position
As a Safety Medical Writer at Novo Nordisk A/S, you will be responsible for planning and managing and preparing aggregate safety documents (Development Safety Update Reports [DSURs], Periodic Safety Update Reports [PSURs], and Clinical Risk Management Plans [RMPs]) and responses to Health Authority questions in a cross-functional environment, ensuring high quality scientific writing.
You will work in close collaboration with Safety Surveillance Advisors, Medical Specialists from Global Development, Medical Advisors from Medical Affairs, Project Managers from Regulatory Affairs, and Safety Publishers.
While your key responsibilities will include preparing the key safety reporting documents you will also be expected to actively contribute to process improvements and other opportunities for increasing efficiency - for example automation of administrative steps.
We are offering a temporary position, for at least 12 months.
Qualifications
You either hold a higher degree in a biological/pharmaceutical science/medicine (PhD, MSc or equivalent), or have equivalent work experience in the medical or pharmaceutical field. Aside from this, you have a demonstrated aptitude and genuine interest in scientific communication and strong command of English.
You must have a good eye for detail and logical structure, you are used to working with datasets and consider yourself to have strong analytical competencies. An understanding of drug safety during drug development would be an advantage.
You thrive in a multicultural environment of continuous development and you are good at establishing contact, communicating, collaborating with colleagues, as well as challenging them. You have strong planning, and project management skills. You are analytical and able to present in a structured, clear and accurate way. You have high ethical standards and are able to prioritise your tasks and rise to challenges.
You are fluent in both written and spoken English (the business language), and an experienced user of MS Office.
Working at Novo Nordisk
At Novo Nordisk your skills, commitment and ambition help us change patients’ lives, for the better. In exchange, we offer you a chance to work with extraordinary talent and to develop professionally and personally.
Contact
For further information, please contact Marcus Schartau (+45) 30 75 67 13.
Deadline
17th November 2020.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 12.11.2020, 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.
- Øvrige
- Bagsværd
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