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Medical Writing Specialist in R&D - Global Development - Denmark  

Novo Nordisk (company)

Posted on : 08 March 2017

Project Description

Requisition ID 45091BR Title Medical Writing Specialist in R&D - Global Development Job Category Research & Development Job Description Are you an experienced Medical Writer looking for possibilities to grow your career further?Then you might be our next Medical Writing Specialist.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 Writing Specialist, your main task is to drive the preparation of complex clinical documents. You will plan and coordinate activities in a cross-disciplinary setting and collaborate with many internal stakeholders in our global organisation. In addition to your own medical writing tasks, you will develop and improve our internal processes, and promote the sharing of better practices across areas. As a specialist, you will mentor and train other medical writers and be responsible for the document quality in your team, as well as your own documents.QualificationsYou have a Master s degree within natural sciences (M.Sc., M.Sc. Pharm. or equivalent), preferably supplemented with a PhD and "e5 years of relevant experience in the pharmaceutical industry. You have a track record of driving your own complex tasks from start to end, navigating many different stakeholders and are an expert in communicating scientific information. You can demonstrate your ability to improve processes and to promote the sharing of better practices. You have expert understanding of 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. 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. You are a clear communicator and a strong team player who adapts easily to a changing environment with tight deadlines. You are strategic, proactive, and have excellent planning skills and coordination skills. You effectively manage various stakeholders and are able 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 Victoria Fuller-Mikkelsen on +45 3075 5726.Deadline24 March 2017.  State/Provinces Denmark Position Location Denmark - S


Denmark Søborg

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