BrightOwl Loader Loading

Medical Writer in R&D  Global Development - Denmark  

Novo Nordisk (company)

Posted on : 08 March 2017

Project Description

Requisition ID 45301BR Title Medical Writer in R&D  Global Development Job Category Research & Development Job Description Clinical Reporting is looking for a Medical Writer.It is a challenging job with significant responsibility in a dynamic, international atmosphere. About the departmentClinical Reporting is the medical writing function at Novo Nordisk and is part of Global Development. We are more than 80 employees, primarily medical writers and clinical publishers, from diverse cultural and professional backgrounds, working in a pleasant and informal atmosphere. We are responsible for preparing clinical documents for submission to regulatory authorities worldwide. The positionAs Medical Writer, your main tasks are writing regulatory clinical documents such as clinical trial reports, investigator s brochures, summary documents and other documents covering interpretation and documentation of clinical data. As we cover all clinical development projects within Novo Nordisk s different therapy areas, the focus and daily tasks depend on the type of document and the life cycle stage of the project. Planning and coordination of activities in a cross-disciplinary setting is also a central part of the job, and we expect that you are capable of driving the writing process and manage relevant stakeholders. The job is globally oriented and requires close collaboration with colleagues in other skill areas in Denmark and abroad. All documents are written in English and must comply with internal Novo Nordisk standard operating procedures and external guidelines. QualificationsYou have a university degree within Natural Sciences (M.Sc., M.Sc. Pharm. or equivalent) including skills within Statistics and scientific research methods. Preferably you have developed your scientific research methods and scientific writing skills by completing a Ph.D. As all of our documents are prepared in English, you master written and spoken English at a professional level, and you have a flair and interest for 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 and managing stakeholders to reach consensus. You are thorough, structured and conscientious, and you have a good sense of humour. Working at Novo NordiskAt 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. In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to market authorisation. We ensure medical and scientific documentation for clinical submissions while ensuring that the process lives up to global standards, regulations and business ethics. ContactFor further information please contact Helle Harder Birkeslund on +45 3077 6632.   Deadline24 March 2017. State/Provinces Denmark Position Location Denmark - S


Denmark Søborg

Find a Job Find a Candidates

Similar jobs

Novo Nordisk company's more jobs

Other jobs in Denmark

Other jobs in Søborg

Other jobs from Novo Nordisk company's in Søborg

Other similar job in Søborg

Other links

Most Recent Searches

Most Famous Searches

you might also likes