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stillingsbetegnelse: Clinical Trial Administrator

jobbeskrivelse:

Global Development, Søborg, Denmark

Do you want to be part of a dynamic team, working in an international environment that drives clinical trial activities? In Biopharm Trial Operations, we are looking for a new colleague to join us working as Clinical Trial Administrator. 

The Biopharm Project is part of 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. 

About the department

Biopharm Trial Operations, is responsible for the set-up and execution of phase 2-4 clinical trials. We are a large area of approximately 70 enthusiastic colleagues such as International Trial Managers, Clinical Trial Administrators and Clinical Project Managers divided into 5 departments. 

Our environment is characterised by a vast global network, knowledge sharing, talented colleagues and challenging assignments in a dynamic project centric organisation. We offer continuous personal and professional development opportunities as being part of a large headquarter function. 

The Job

As Clinical Trial Administrator you will be an essential member of the trial team supporting the clinical trial planning, execution and finalisation by performing administrative tasks as well as wide communication with international stakeholders and collaborators.

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 (SOP) 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 IT Clinical systems as well as IT project tools.

In addition, you will process invoices and support preparation and updating of trial budgets.

As a Clinical Trial Administrator, you will set up and maintain the web-portal used by the International Study Group for sharing trial related documents as well as support and prepare newsletters and PowerPoint presentations.

You will contribute to successful international meetings on Skype as well as face to face by coordinating the logistics, ensuring applicable equipment available, and other tasks that enable the International Trial Manager to focus on the content and outcome.

 

QualificationsYou have broad administrative experience from supportive roles during your career. It is an advantage if you already have experience from working in a regulated industry and/or are familiar with document management. You are proficient with both written and spoken English, have a flair for using IT systems and are highly skilled within MS Office, including Excel. 

Our ideal candidate has a strong customer service mind-set, is able to independently organise tasks and is well structured with a sense for detail and a good overview at the same time. It is important that you can manage deadlines and can work with multiple and frequently changing priorities using good collaboration skills and a sense of humour. 

Working at Novo Nordisk

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

 

Contact

For further information please contact Head of Trial Ops.1, Majbritt Hufeldt +45 3075 6840 

Deadline

17-March-2019 

Millions rely on usTo 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/C3111

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