International Trial Manager, Maternity vacancy
- Research & Development
- Denmark - Søborg
If you are driven by taking responsibility for the planning and execution of clinical trials within quality, timeline and budget deliverables, you may be our new International Trial Manager.
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, 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
We are seeking a new colleague to take up a temporary position as International Trial Manager for 10 months. As International Trial Manager you will be responsible for timely planning, executing and finalizing clinical trials using your operational and therapeutic experience. You will be leading the trial team and coordinate trial management activities in order to meet key deliverables and quality standards. Tasks will be solved through proactive planning, team work, clear communication and stakeholder management. You will be a main contributor during international meetings requiring you to have strong cross-cultural awareness and presentation skills. Your main responsibility will be the development of critical trial documents like the trial protocol, the clinical operational plan and the trial budget which will require you to have an eye for important details while keeping the overview. You will be expected to digest complex data outputs, analyse complex scientific challenges and to ensure a high level of quality in all you do.
Qualifications
You hold a university degree in health, biological, pharmaceutical science or equivalent with preferably two years of experience in trial or project management related positions. You have a broad knowledge of clinical trial methodology and you have excellent presentation, organizational and cooperation skills. A quality mind set is a must, together with a focus on meeting deadlines, communicating effectively and maintaining overview. You have a determined, analytic and structured personality with a pragmatic and quality based approach to your tasks. You strive in a dynamic and challenging cross-cultural environment and you are motivated by leading a team and developing solutions to complex challenges. You are an experienced IT user and capable of familiarizing yourself with advanced technologies. You are a dedicated team player with a natural drive and motivation who inspires trust and engagement amongst colleagues and partners. Fluency in written and spoken English is essential.
At Novo Nordisk, we strive for excellence. As a world leading pharmaceutical company, we offer our employees opportunities for continuous personal development and excellent career opportunities.
Contact
For further information, please contact Iris Koenig at+45 3079 3971 or Lars Bjørn Justesen at +45 3079 6501.
Deadline
12 January 2014
- Research & Development
- Denmark - Søborg
If you are driven by taking responsibility for the planning and execution of clinical trials within quality, timeline and budget deliverables, you may be our new International Trial Manager.
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, 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
We are seeking a new colleague to take up a temporary position as International Trial Manager for 10 months. As International Trial Manager you will be responsible for timely planning, executing and finalizing clinical trials using your operational and therapeutic experience. You will be leading the trial team and coordinate trial management activities in order to meet key deliverables and quality standards. Tasks will be solved through proactive planning, team work, clear communication and stakeholder management. You will be a main contributor during international meetings requiring you to have strong cross-cultural awareness and presentation skills. Your main responsibility will be the development of critical trial documents like the trial protocol, the clinical operational plan and the trial budget which will require you to have an eye for important details while keeping the overview. You will be expected to digest complex data outputs, analyse complex scientific challenges and to ensure a high level of quality in all you do.
Qualifications
You hold a university degree in health, biological, pharmaceutical science or equivalent with preferably two years of experience in trial or project management related positions. You have a broad knowledge of clinical trial methodology and you have excellent presentation, organizational and cooperation skills. A quality mind set is a must, together with a focus on meeting deadlines, communicating effectively and maintaining overview. You have a determined, analytic and structured personality with a pragmatic and quality based approach to your tasks. You strive in a dynamic and challenging cross-cultural environment and you are motivated by leading a team and developing solutions to complex challenges. You are an experienced IT user and capable of familiarizing yourself with advanced technologies. You are a dedicated team player with a natural drive and motivation who inspires trust and engagement amongst colleagues and partners. Fluency in written and spoken English is essential.
At Novo Nordisk, we strive for excellence. As a world leading pharmaceutical company, we offer our employees opportunities for continuous personal development and excellent career opportunities.
Contact
For further information, please contact Iris Koenig at+45 3079 3971 or Lars Bjørn Justesen at +45 3079 6501.
Deadline
12 January 2014
