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stillingsbetegnelse: Safety Medical Writer

jobbeskrivelse:

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 Surveillance Reporting 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 educational background within natural science. Safety Surveillance Reporting is responsible for reporting the surveillance of all safety information for Novo Nordisk’s products, that are currently marketed or under development worldwide, to ensure patient safety.

 

The position

As a Safety Medical Writer in Safety Surveillance Reporting at Novo Nordisk A/S, you will be responsible for planning and managing document preparation (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 and 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 projects, for example we are currently looking into possibilities for auto-population in documents.

 

Qualifications

You hold a university degree in a biological/pharmaceutical science/medicine and have a demonstrated aptitude and genuine interest in scientific communication, in English. You must have a good eye for detail and logical structure. 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 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 Rachael Profit (+45) 30 79 95 20.

 

Deadline

29 April 2019 

 

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 chronical 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.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C8131

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: NOVO NORDISK A/S

source: DK-STAR