id: NDk1OTE5MCA3

reference: 4959190

documentId: 4959190

connectionPointId: 7

lastModificationDate: 1552466942250

stillingsbetegnelse:
Clinical Trial Administrator in Obesity Trial Operations

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 Obesity Trial Operations, we are looking for a new colleague to join as Clinical Trial Administrator. 

The Obesity 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.

 

About the department

Obesity Trial Operations, is responsible for the set-up and execution of phase 2-4 clinical trials. We are a large area of approximately 40 enthusiastic colleagues divided into 3 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) including uploading and updating of information, indexing and Quality Control of trial documents in our different IT Clinical systems as well as IT project tools. 

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 set up international meetings on Skype as well as face to face by coordinating the logistics.

 

Qualifications
You have broad administrative experience from supportive roles during your career preferably within the pharmaceutical industry. 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, can 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 Director, Lone Petersen +45 3075 0947

 

Deadline

24-March-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/C2421

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