Clinical Trial Administrator in GLP-1, CV & Outcomes, Trial Operations
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Søborg
- Clinical Development and Medical
- Søborg
Global Development, Søborg, Denmark
Do you want to be part of a dynamic team, working in an international environment that drives clinical trial activities? Are you structured and have good planning skills? Do you have a passion for administrative and coordinating tasks? Then we may have just the right job for you!
In Global Development, GLP-1, CV & Outcomes, Trial Operations, we are looking for a new colleague to join as Clinical Trial Administrator.
About the department
GLP-1, CV & Outcomes, Trial Operations, is responsible for the set-up and execution of phase 2-4 clinical trials. We are a large area of more than 60 enthusiastic colleagues 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 management 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 virtual international meetings on Microsoft Teams as well as face to face meetings and maintain a web-portal used by the trial team members for sharing trial related documents, prepare newsletters and PowerPoint presentations.
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 and Teams. It will also be an advantage if you have knowledge with Trial Master File systems.
Our ideal candidate is a strong team player, can work independently 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. You have 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 Manager, Winnie Søjborg Sussoh +45 3075 0821
Deadline
22-March-2020
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.
Information og data
Denne ledige stilling har jobtypen "Jurist", og befinder sig i kategorien "Økonomi og jura".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 6.3.2020, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Jurist
- Søborg
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