International Trial Manager
- Research & Development, Trial Manager
- Denmark - Søborg
Clinical Operations, Degludec is looking for a candidate to join us working as International Trial Manager.By joining us you will be offered vast responsibilities and opportunities to increase your experience within trial management and to develop your competences within a clinical trial life cycle ranging from planning and preparation through execution to finalisation of large scale phase 3 studies.
About the department
We are a team of experienced and enthusiastic Clinical Project Managers, International Trial Managers and Clinical Trial Administrators who are responsible for planning and conducting clinical trials within the diabetes area, in close collaboration with Novo Nordisk affiliates all over the world. Our work environment is characterised by exciting new challenges, a global network, knowledge sharing and 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 function as a global project manager for trial activities by using your operational and therapeutic expertise. You will coordinate trial management activities in a proactive fashion through clear communication and great team work.As 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 Investigator and Monitor meetings. You will use a structured and analytic approach during development of the trial protocol and other relevant trial documents such as informed consent, recruitment strategies, risk analysis plan, communication plans etc. You have an eye for important details and at the same time keep the overview, digest complex data output and evaluate the adequate level of quality.You have the ability to drive the progress of trial activities within given timelines and in accordance with the trial budget that you prepare and keep updated.
Qualifications
You hold a university degree in medical, biological, pharmaceutical science or equivalent with several years of experience in trial management related positions. You have a broad knowledge of clinical trial methodology and experience from working in a project organisation.You have a quality mindset, meet your deadlines, communicate effectively with high impact, and can prioritise your work 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. Fluency in written and spoken English as well as experienced user of Microsoft Office and an interest in IT is essential.
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, please contact Hans Henrik Friberg on +45 3079 6626.
Deadline
26 July 2013.
- Research & Development, Trial Manager
- Denmark - Søborg
Clinical Operations, Degludec is looking for a candidate to join us working as International Trial Manager.By joining us you will be offered vast responsibilities and opportunities to increase your experience within trial management and to develop your competences within a clinical trial life cycle ranging from planning and preparation through execution to finalisation of large scale phase 3 studies.
About the department
We are a team of experienced and enthusiastic Clinical Project Managers, International Trial Managers and Clinical Trial Administrators who are responsible for planning and conducting clinical trials within the diabetes area, in close collaboration with Novo Nordisk affiliates all over the world. Our work environment is characterised by exciting new challenges, a global network, knowledge sharing and 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 function as a global project manager for trial activities by using your operational and therapeutic expertise. You will coordinate trial management activities in a proactive fashion through clear communication and great team work.As 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 Investigator and Monitor meetings. You will use a structured and analytic approach during development of the trial protocol and other relevant trial documents such as informed consent, recruitment strategies, risk analysis plan, communication plans etc. You have an eye for important details and at the same time keep the overview, digest complex data output and evaluate the adequate level of quality.You have the ability to drive the progress of trial activities within given timelines and in accordance with the trial budget that you prepare and keep updated.
Qualifications
You hold a university degree in medical, biological, pharmaceutical science or equivalent with several years of experience in trial management related positions. You have a broad knowledge of clinical trial methodology and experience from working in a project organisation.You have a quality mindset, meet your deadlines, communicate effectively with high impact, and can prioritise your work 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. Fluency in written and spoken English as well as experienced user of Microsoft Office and an interest in IT is essential.
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, please contact Hans Henrik Friberg on +45 3079 6626.
Deadline
26 July 2013.