Clinical Trial Administrator

NÁPLŇ PRÁCE:

- Administrative - Denmark - Søborg Do you want to assist a dynamic team that drives clinical trial activities in an international setting? In Clinical Operations, Insulin & Diabetes Outcomes, we are looking for a new colleague to join one of our departments, ClinOps 2, as a Clinical Trial Administrator in a temporary position in Søborg until 1st May 2016. About the department Clinical Operations Insulin and Diabetes Outcomes is a department within the Insulin & Diabetes Outcomes project in Global Development. In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to product introduction. We ensure medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to uniform global standards, regulations and business ethics. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society. Clinical Operations is responsible for planning and conducting clinical trials within the diabetes area from phase 2-4. As Clinical Trial Administrator you will play a key role in coordinating activities within ClinOps and Novo Nordisk affiliates all over the world. The department consists of a well-established team of experienced and enthusiastic Clinical Trial Administrators, International Trial Managers and a Clinical Project Manager. The job You will support the team of International Trial Managers that is responsible for the management of our global clinical trials. You will contribute to successful meetings by coordinating and planning the logistics, ensuring availability of applicable equipment, completion of minutes and general support that enables the International Trial Manager to focus on the content and outcome. You will set up and maintain the shared web sites used by the International Study Group for sharing trial related documents as well as contribute to the preparation of newsletters and PowerPoint presentations. By use of your structured approach and high quality mindset you will establish and maintain the Trial Master Files in accordance with standard operational procedures and in close collaboration with the International Trial Managers. This also includes uploading, updating of information, indexing and quality control of trial documents in our different clinical IT systems as well as IT project tools. In addition, you will support the trial team with ad hoc office tasks as needed. Qualifications You have at least 2-3 years of experience in an administrative position, preferably within the pharmaceutical industry. You are proficient with both written and spoken English. You have flair for using IT systems and you are highly skilled within MS Office. The ideal candidate will have a strong customer service mindset, be able to independently organise the work and is well structured with a sense for detail and a good overview at the same time. You like being part of a multi-cultural team. It is important that you can manage deadlines and work with multiple and frequently changing priorities using good collaboration skills and a sense of humour. Working at Novo Nordisk Novo Nordisk is a world leader in diabetes care. Our success is built on more than 90 years of innovation and commitment to patient-care. We combine world-class scientific, pharmaceutical, and clinical expertise with the highest ethical standards to continue to improve the quality of life of millions of patients across the world. Contact For further information, please contact Line Elmøe Glesner on +45 3075 1950. Deadline 24 September 2015.

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source: https://www.ec.europa.eu/eures

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