Vice President of Clinical Quality
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Søborg
Are you ready for a life-changing career at Novo Nordisk? Working at Novo Nordisk is never just a job, it is an opportunity to have a life-changing career – you grow professionally, and you impact the lives of our patients for better. Novo Nordisk is a global healthcare company with more than 100 years of driving change for better health and is headquartered in Denmark. Our purpose is to drive change to defeat serious chronic diseases such as diabetes, obesity and rare diseases. We employ more than 59,000 people in 80 offices around the world, and market our products in 170 countries.In the R&D organisation we are currently looking for a VP of Clinical Quality who will be overall responsible for leading quality-related activities for clinical development, driving sustainable and innovative solutions involving enterprise-wide collaboration, as well as developing and leading long- and short-term business strategies within the organisation.
About the department
R&D Quality is part of the SVP area Submissions and Lifecycle Management. In R&D Quality we play a key role in how we execute on the R&D strategy in collaboration across functional lines. We work closely with our business partners in Research and Development, which includes Clinical Drug Development, Data Science, Device & Delivery Solutions, Regulatory Affairs, Global Safety as well as with our CMR colleagues around the world. We are securing that processes live up to uniform global standards, regulations and business ethics, thereby safeguarding patient safety and our license to operate globally. Clinical Quality is one of five departments in R&D Quality.The position
Based in Søborg, Denmark, you will report directly to the Corporate Vice President for R&D Quality and lead an organisation of 5 direct reports with a total of 35+ employees. In your role as VP Clinical Quality you will lead and orchestrate strategic priorities and transformation in the organisation and in the way by which the business is positioned.
In your role, you will also be responsible for setting strategic direction together with Process Owners and Delegates and ensure compliance with internal as well as external clinical regulations and requirements globally as Process QA.Moreover, you will represent Novo Nordisk and R&D Quality in external networks to establish strong collaboration with peer companies and influence external expectations (e.g., inspections) and ways of working.As key accountabilities, you will be responsible for:Leadership role modelEfficiently lead organisational changes, development, communication and training in line with Novo Nordisk Way securing enterprise-wide collaboration, high engagement as well as development of the team. Secure that all areas in the VP function are in compliance with Novo Nordisk guidelines covering quality and compliance.Business development
Ensure that the Clinical Quality area at any time has a solid organisational structure, processes and competencies to lead the clinical quality support to our stakeholders globally as well as securing a sustainable, future business.
Strategic responsibilities within the VP area
Responsible for driving and leading strategy, innovation and simplification and for fostering a strong quality mind-set and cultureLeadership and day to day operations
Ensure the VP Area delivers according to the Novo Nordisk annual wheel for LoB activities, lead organisational performance management, including feedback and rewards, proactively secure resource planning, continuous improvement including digitalisation, budget targets management, Occupational Health & Safety.
Qualifications
Outstanding Leadership and communication skills. You hold a Master’s degree in science (e.g. M.Sc, MD, DVM), +15 years’ experience in drug development and +10 years’ experience with line management with Leadership experience within clinical development, clinical quality & compliance plus significant experience with external collaborations, comprehensive knowledge of industry drug development and proven track record of creating business results with impact on SVP/EVP level.
Strong communication skills in English (verbally and in writing) is a must.Deadline
24 November, 2023.
Important note: be aware that our systems will have programmed downtime that will prevent applications from Friday, November 17, to Saturday, November 18.You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.Contact
If you require further information about the role, please contact Executive Search Partner, Fabio Marra at [email protected] We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
About the department
R&D Quality is part of the SVP area Submissions and Lifecycle Management. In R&D Quality we play a key role in how we execute on the R&D strategy in collaboration across functional lines. We work closely with our business partners in Research and Development, which includes Clinical Drug Development, Data Science, Device & Delivery Solutions, Regulatory Affairs, Global Safety as well as with our CMR colleagues around the world. We are securing that processes live up to uniform global standards, regulations and business ethics, thereby safeguarding patient safety and our license to operate globally. Clinical Quality is one of five departments in R&D Quality.The position
Based in Søborg, Denmark, you will report directly to the Corporate Vice President for R&D Quality and lead an organisation of 5 direct reports with a total of 35+ employees. In your role as VP Clinical Quality you will lead and orchestrate strategic priorities and transformation in the organisation and in the way by which the business is positioned.
In your role, you will also be responsible for setting strategic direction together with Process Owners and Delegates and ensure compliance with internal as well as external clinical regulations and requirements globally as Process QA.Moreover, you will represent Novo Nordisk and R&D Quality in external networks to establish strong collaboration with peer companies and influence external expectations (e.g., inspections) and ways of working.As key accountabilities, you will be responsible for:Leadership role modelEfficiently lead organisational changes, development, communication and training in line with Novo Nordisk Way securing enterprise-wide collaboration, high engagement as well as development of the team. Secure that all areas in the VP function are in compliance with Novo Nordisk guidelines covering quality and compliance.Business development
Ensure that the Clinical Quality area at any time has a solid organisational structure, processes and competencies to lead the clinical quality support to our stakeholders globally as well as securing a sustainable, future business.
Strategic responsibilities within the VP area
Responsible for driving and leading strategy, innovation and simplification and for fostering a strong quality mind-set and cultureLeadership and day to day operations
Ensure the VP Area delivers according to the Novo Nordisk annual wheel for LoB activities, lead organisational performance management, including feedback and rewards, proactively secure resource planning, continuous improvement including digitalisation, budget targets management, Occupational Health & Safety.
Qualifications
Outstanding Leadership and communication skills. You hold a Master’s degree in science (e.g. M.Sc, MD, DVM), +15 years’ experience in drug development and +10 years’ experience with line management with Leadership experience within clinical development, clinical quality & compliance plus significant experience with external collaborations, comprehensive knowledge of industry drug development and proven track record of creating business results with impact on SVP/EVP level.
Strong communication skills in English (verbally and in writing) is a must.Deadline
24 November, 2023.
Important note: be aware that our systems will have programmed downtime that will prevent applications from Friday, November 17, to Saturday, November 18.You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.Contact
If you require further information about the role, please contact Executive Search Partner, Fabio Marra at [email protected] We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 10.11.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Søborg
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