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UDLØBET

Novo Nordisk

Clinical Trial Administrator / Senior Clinical Trial Administrator

Fuldtid

Permanent

Gladsaxe

SE PÅ KORT
ID: 2421792
|
Indrykket for 117 dage siden

Area: Clinical Drug Development, Clinical Operations, OSCD & Outcomes

Are you interested in being part of a dedicated team driving clinical activities in an international setting? Are you passionate about clinical research and would like to be closer to the newest development of new medicines for millions of patients. Are you just as good at handling documents as you are handling stakeholders across professions, geography, and cultures? Are you structured and have good planning skills, and do you have a passion for administrative and coordinating tasks? Then we may have just the right job for you! In Clinical Drug Development, Clinical Operations, we are looking for a new colleague to join as Clinical Trial Administrator.

About the area

In our project area we cover the entire spectrum of clinical development activities within Cardiovascular Disease, Chronic Kidney Disease and Alzheimer Disease from early phase 1 trials to large phase 3a programs and phase 3b/4 life cycle management activities on our marketed products.

In Clinical Operations we are responsible for the set-up and execution of phase 1-4 clinical trials within the area. Our environment is characterised by a vast global network and collaboration, 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 Position

As Clinical Trial Administrator you will be an essential member of the trial management team providing administrative support on the clinical trials in all relevant aspects of preparation, conduct, documentation, and archiving.

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 (SOPs) including uploading and updating of information, indexing and Quality Control of trial documents in our different IT Clinical systems.

You will be highly involved in outsourcing processes, trial budgets and you will assist in updating clinical documents such as protocol and protocol amendments and be involved in the preparation of monitoring guidelines, laboratory manuals, and patient enrolment updates. All activities are carried out in close collaboration with the responsible trial managers. Finally, you will support meeting planning and you will be collaborating with both internal and external stakeholders worldwide. The position is based in Søborg, Denmark.

For the right external candidate this position may be upgrade to a senior position.


Qualifications

To succeed in this role, you should have the following qualifications:

Have broad administrative experience from supportive roles during your career, preferably within the pharmaceutical industry.


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 and you are proficient with both written and spoken English
 

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