Novo Nordisk A/S
Gladsaxe, 1 stilling
- Administrative
- Denmark - Søborg
If you are motivated by supporting the planning and execution of clinical trials within quality-, timeline- and budget deliverables, you may be our new Clinical Trial Administrator (CTA) in Haemophilia, Clinical Operations.
About the Department
Haemophilia, Clinical Operations is a team of 70 highly skilled and ambitious colleagues responsible for planning and execution of clinical trial activities, hereby securing Novo Nordisk a world leading position within the treatment of haemophilia and rare bleeding disorders. The scope of our activities is phase 1 to 4 clinical trials in collaboration with our Novo Nordisk affiliates. Being a headquarter division our environment is characterised by a vast global network with high quality standards, challenging assignments and continuous career opportunities.
The Job
Each clinical trial must be conducted according to agreed targets for time and cost and to excellent quality standards in order to ensure approval of the drug. The CTA supports this goal and has a significant role in trial planning and execution by supporting the International Trial Managers with trial related tasks in a proactive and independent manner. The CTA acts as a coordinator for the study team, including coordination of trial activities in collaboration with colleagues at Novo Nordisk affiliates worldwide.
Further, the CTA establishes trial master files according to Novo Nordisk Standard Operational Procedures, prepares and maintains trial documents and files. The CTA compiles, archives, creates and imports documents in an internal electronic archive, carries out quality checks and finalises documents. The CTA also supports the study team in meeting planning, execution, and taking meeting minutes.
The responsibilities also include preparation and updates of the trial budgets in collaboration with the International Trial Managers. The CTA coordinates trial newsletters and maintains websites as applicable, and finally updates trial information in relevant clinical IT systems (e.g. IMPACT), and prepares trial updates to management.
Qualifications
Your educational background could include a bachelor degree, preferably within IT or science, with at least two years of experience with similar tasks in the medical/pharmaceutical industry. Fluent in written and spoken English. Team oriented personality with high degree of flexibility and cross-cultural awareness, good communication skills, systematic with attention to details, responsible, preferably a good understanding of project management. Ability and willingness to adjust quickly to new situations in a continuously developing environment. Experienced user of Microsoft Office Package (Outlook, Word, Excel, PowerPoint), preferably with a general flair for IT systems.
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 Helle Lundholm at +45 3079 4302 or Anita Borup Helboe at +45 3079 1571.
Deadline
22 October 2015.
