Director Medical Anchor
- Research & Development
- Denmark - Søborg
Are you passionate about developing people and processes and do you have visions and ideas for the Medical Specialists working with drug development? We are seeking a Director of Medical Anchor .
In this position, you will be responsible for the global medical competency development and key medical processes owned by Trial Execution and you will have the line management responsibilities of 6 employees in your department.
You can look forward to a high impact and very diverse position. You will collaborate globally with a wide range of Novo Nordisk colleagues across the organisation and you will chair the medical management councils. The span of the position is in Global Development, across R&D and in several functional areas in Novo Nordisk outside of R&D such as the CMR regions, Medical Affairs and Global Safety.
About the department
Trial Execution is the skill area for Medical and Trial Management anchored in Global Development in Søborg. We are a team of 21 dedicated employees of diverse background, with a shared interest in clinical trial optimisation and competency building within medical and trial management globally. We work in close collaboration with many functions as described above.
The job
As Director of the department you will report to the Vice President of Trial Execution, Clinical Operation in Søborg. You will lead a team of 6 specialists with long-standing experience of process optimisation and responsible for global support and maintenance of key clinical trial processes e.g. Safety Adjudication, Clinical Development Plan (CDP), Trial Outline, HCP HTR and mynovotrial.com.
You will be overall responsible for setting the strategic direction to meet future business needs from a medical perspective together with the Heads of Medical & Science in the Key Projects. You will chair medical management councils as HQMedManCouncil and GlobalMedManCouncil, drive relevant focus areas and ensure knowledge sharing across projects and regions within the medical area
You will be contributing to improving global medical and medically related cross-functional processes, and you will represent the Medical Specialists in selected cross-functional teams. You will also be responsible for a proactive approach in building knowledge and competences within the Medical Specialist community.
Qualifications
This is a high impact position, and as such requires seniority. You hold an academic degree e.g. MD, which you have supplemented with programmes in management and business development. You have proven experience with and insight into planning and conducting international clinical programmes. You have a thorough understanding of the pharmaceutical business and you have a drive for impacting improvement projects and processes which requires profound medical, scientific and drug development knowledge. You have solid leadership experience, including leading multinational and cross-functional teams.
The job requires networking ability, working across boundaries and excellence in stakeholder management. You possess excellent communication and presentation skills. Interactions with internal and external experts require proficiency in English. You are well structured, combine high analytical skills with result focus. You are change-prepared and you have a proactive mind-set.
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 Eva Åsbrink Nilsson +45 3075 1547.
Deadline
23 September 2013.
- Research & Development
- Denmark - Søborg
Are you passionate about developing people and processes and do you have visions and ideas for the Medical Specialists working with drug development? We are seeking a Director of Medical Anchor .
In this position, you will be responsible for the global medical competency development and key medical processes owned by Trial Execution and you will have the line management responsibilities of 6 employees in your department.
You can look forward to a high impact and very diverse position. You will collaborate globally with a wide range of Novo Nordisk colleagues across the organisation and you will chair the medical management councils. The span of the position is in Global Development, across R&D and in several functional areas in Novo Nordisk outside of R&D such as the CMR regions, Medical Affairs and Global Safety.
About the department
Trial Execution is the skill area for Medical and Trial Management anchored in Global Development in Søborg. We are a team of 21 dedicated employees of diverse background, with a shared interest in clinical trial optimisation and competency building within medical and trial management globally. We work in close collaboration with many functions as described above.
The job
As Director of the department you will report to the Vice President of Trial Execution, Clinical Operation in Søborg. You will lead a team of 6 specialists with long-standing experience of process optimisation and responsible for global support and maintenance of key clinical trial processes e.g. Safety Adjudication, Clinical Development Plan (CDP), Trial Outline, HCP HTR and mynovotrial.com.
You will be overall responsible for setting the strategic direction to meet future business needs from a medical perspective together with the Heads of Medical & Science in the Key Projects. You will chair medical management councils as HQMedManCouncil and GlobalMedManCouncil, drive relevant focus areas and ensure knowledge sharing across projects and regions within the medical area
You will be contributing to improving global medical and medically related cross-functional processes, and you will represent the Medical Specialists in selected cross-functional teams. You will also be responsible for a proactive approach in building knowledge and competences within the Medical Specialist community.
Qualifications
This is a high impact position, and as such requires seniority. You hold an academic degree e.g. MD, which you have supplemented with programmes in management and business development. You have proven experience with and insight into planning and conducting international clinical programmes. You have a thorough understanding of the pharmaceutical business and you have a drive for impacting improvement projects and processes which requires profound medical, scientific and drug development knowledge. You have solid leadership experience, including leading multinational and cross-functional teams.
The job requires networking ability, working across boundaries and excellence in stakeholder management. You possess excellent communication and presentation skills. Interactions with internal and external experts require proficiency in English. You are well structured, combine high analytical skills with result focus. You are change-prepared and you have a proactive mind-set.
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 Eva Åsbrink Nilsson +45 3075 1547.
Deadline
23 September 2013.