Senior Trial Manager to run global clinical trials in
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Søborg
- Clinical Development and Medical
- Søborg
Do you have in depth experience in setting up and driving global clinical trials and do you thrive in proactively taking on tasks having individual accountability, share better practise and being a role model in driving agile and fit-for purpose trial execution? Then we have a job for you that will offer you ample opportunities to maintain and develop your skills in a truly global business environment.
About the department
In Global Development, we are responsible for clinical drug development worldwide from early development phases to market approval, as well as life cycle management. We ensure medical and scientific documentation for clinical submissions to authorities. Our main focus is on delivering products that make a difference to patients with diabetes, obesity and rare diseases.
In Biopharm Trial Operations, we are responsible for the planning, execution and finalisation of global clinical trials in phase 2-4 within non-malignant haematology and rare endocrine disorders. We are organised in global project teams. We value an open, trust-based and creative working environment, great team spirit and a high-quality mind-set and with continuous professional development opportunities.
The position
As senior TMs you are responsible for planning, execution and finalisation of clinical trials in accordance with project goals.
You will be part of setting up trials, developing trial documentation and manuals, recruitment and retention strategies, providing input to clinical IT systems and planning and conducting Monitor and Investigator meetings.
Through clear communication and teamwork, you ensure delivery of trial management activities and coordinate deliverables from relevant stakeholders as well as keep track of trial risks and mitigation plans. You engage independently with external vendors, internal stakeholders across skill areas and our colleagues in the Novo Nordisk affiliates worldwide.
Qualifications
You have a MSc/BSc in Natural Science or equivalent with at least 4 years of experience in trial management as well as clinical trial methodology.
You have solid project management experience and an ability to balance quality with a drive to meet challenging deadlines. In this role it is essential that you make risk-based prioritisation of issues and situational adjustment of tasks and actions. You adjust quickly in a continuously developing environment, where you thrive solving complex challenges. You are structured and have a proven track record of ensuring that trial activities progress within the given timelines and in accordance with the trial budget.
Cross cultural awareness, team spirit and the ability to motivate others in a positive working climate are key to success.
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 Claus Banner at +45 3075 9772
Deadline
26-November-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.
Information og data
Denne ledige stilling har jobtypen "Produktspecialist", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 11.11.2019, 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.
- Produktspecialist
- Søborg
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