International Trial Manager in Semaglutide (temporary position)
International Trial Manager in Semaglutide (temporary position)
Novo Nordisk A/S
Gladsaxe, 1 stilling
- Clinical Trial Management
- Denmark - Søborg
Do you have a passion for driving global clinical trials and do you want to exert your influence by leading large global clinical trials to develop the world’s best diabetes treatments? Then we may have just the right job for you.
Clinical Operations, Semaglutide is looking for an International Trial Manager to join us.
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
In Clinical Operations, Semaglutide we are approximately 60 highly skilled and ambitious employees.
We are responsible for the planning, execution and finalisation of clinical trial activities with subcutaneous and oral semaglutide in phase 2-3. We collaborate with external vendors and our colleagues in the Novo Nordisk affiliates worldwide.
We value an open, trust-based and creative working environment, great team spirit and a high quality mind-set. Our working environment is characterised by interesting and demanding assignments and continuous professional development opportunities.
The position
The job as International Trial Manager demands that you are capable of directing and driving activities within global clinical trials. You will be responsible for ensuring that project key deliverables are met in time, at a high quality and within budget. You will be part of the international study group, where you will contribute to planning and conducting team meetings with focus on stakeholder engagement, knowledge sharing and decision making.
The job requires that you apply a structured and analytical approach during development of relevant trial documents such as trial protocol, informed consent, recruitment strategies, risk analysis plans, communication plans and trial budgets. You are detail-oriented, while able to maintain overview, digest complex data and evaluate the adequate level of quality.
The position is a full time position for 12 months.
Qualifications
You hold an academic degree within life sciences or healthcare. You have knowledge of clinical trial planning, execution and finalisation and experience in managing clinical trials. You are a clear communicator and can inspire and motivate a team to deliver their best in an ever-changing environment.
The job requires proficiency in English. You work independently while also being a dedicated team player and you have good cross-cultural awareness.
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 Benedikte Lertoft +45 3079 2893.
Deadline
31 May 2016.
