International Trial Manager
- Research & Development, Trial Manager
- Denmark - Søborg
In this job, 300.000 people worldwide depend on you to develop the world’s best bleeding disorder treatments. If you find challenges like this exciting and inspiring, you may be our new temporary International Trial Manager within our Haemophilia project portfolio.
About the department
Clinical Operations, Haemophilia is a team of 70 highly skilled and ambitious colleagues responsible for planning and execution of clinical trial activities in accordance with the Clinical Development Plans within haemophilia and rare bleeding disorders. The scope of our activities is phase 1 to 4 clinical trials in collaboration with our Novo Nordisk affiliates and Contract Research Organisations. Our environment is characterised by a vast global network with interesting assignments, flexible working conditions, continuous personal and professional development and exciting opportunities which come when working for a large headquarter function.
The job
As International Trial Manager you will be responsible for timely planning, executing and finalizing clinical trials using your operational and therapeutic experience. You will coordinate trial management activities in a proactive fashion through clear communication and good team work. As a chairperson of the international study team you will organise and execute team meetings and ensure the involvement of relevant stakeholders for decision making. You will participate in and contribute to relevant Investigators and Monitor meetings. You have a structured and analytical approach during development of critical trial documents like the trial protocol, and at the same time you have an eye for important details while keeping the overview. You are able to digest complex data output and to evaluate the adequate levels of quality in all you do. By joining us you will get the opportunity to further develop your competencies within trial management in an international environment.
Qualifications
You hold a university degree in medical, biological, pharmaceutical science or equivalent with at least 2 years of experience in trial management related positions. You have a broad knowledge of clinical trial methodology and you have good presentation, communication and negotiation skills. A quality mind set is a must, together with a focus on meeting deadlines, communicating effectively and knowing how to prioritise between different tasks in a dynamic environment. You are a dedicated team player with a high degree of flexibility and cross-cultural awareness who inspires trust amongst colleagues and partners. Fluency in written and spoken English is essential. Experience in running non-interventional studies is of advantage, as well as knowledge of life cycle management.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information regarding this temporary position, please contact Karolina Rask at +45 3079 2670 or Nis Hjortskov Jensen at +45 3079 7857.
Deadline
6 January 2014.
- Research & Development, Trial Manager
- Denmark - Søborg
In this job, 300.000 people worldwide depend on you to develop the world’s best bleeding disorder treatments. If you find challenges like this exciting and inspiring, you may be our new temporary International Trial Manager within our Haemophilia project portfolio.
About the department
Clinical Operations, Haemophilia is a team of 70 highly skilled and ambitious colleagues responsible for planning and execution of clinical trial activities in accordance with the Clinical Development Plans within haemophilia and rare bleeding disorders. The scope of our activities is phase 1 to 4 clinical trials in collaboration with our Novo Nordisk affiliates and Contract Research Organisations. Our environment is characterised by a vast global network with interesting assignments, flexible working conditions, continuous personal and professional development and exciting opportunities which come when working for a large headquarter function.
The job
As International Trial Manager you will be responsible for timely planning, executing and finalizing clinical trials using your operational and therapeutic experience. You will coordinate trial management activities in a proactive fashion through clear communication and good team work. As a chairperson of the international study team you will organise and execute team meetings and ensure the involvement of relevant stakeholders for decision making. You will participate in and contribute to relevant Investigators and Monitor meetings. You have a structured and analytical approach during development of critical trial documents like the trial protocol, and at the same time you have an eye for important details while keeping the overview. You are able to digest complex data output and to evaluate the adequate levels of quality in all you do. By joining us you will get the opportunity to further develop your competencies within trial management in an international environment.
Qualifications
You hold a university degree in medical, biological, pharmaceutical science or equivalent with at least 2 years of experience in trial management related positions. You have a broad knowledge of clinical trial methodology and you have good presentation, communication and negotiation skills. A quality mind set is a must, together with a focus on meeting deadlines, communicating effectively and knowing how to prioritise between different tasks in a dynamic environment. You are a dedicated team player with a high degree of flexibility and cross-cultural awareness who inspires trust amongst colleagues and partners. Fluency in written and spoken English is essential. Experience in running non-interventional studies is of advantage, as well as knowledge of life cycle management.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information regarding this temporary position, please contact Karolina Rask at +45 3079 2670 or Nis Hjortskov Jensen at +45 3079 7857.
Deadline
6 January 2014.