Principal Digital Quality Specialist
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Søborg
Are you motivated by the pursuit of greater data transparency, benefiting patients, healthcare professionals (HCPs), and our Novo Nordisk trial team as we advance dose titration? Are you prepared to take the helm of our ePID (Electronic Patient Interaction Device), guiding the quality roadmap and streamlining processes to adhere to regulatory standards? Then this is your chance to join us as Principal Digital Quality Specialist in the ePID team. Apply now and join our digital transformation journey in Clinical Drug Development! The position The primary functions of the ePID solution are to collect, display, store, process, and transfer clinical trial-related data and to support dose titration. The functions are configurable in the way that connected devices are the key to data collection and can vary depending on trial needs. The connected devices capture data from patients, which the patient can view, verify, and submit instantly on the app interface, sharing simultaneously with HCPs responsible for trial conduct. HCPs use the web interface to monitor and track trial progress. As Principal Digital Quality Specialist, you will assume a pivotal position in the ePID team, spearheading a culture of unwavering commitment to quality. Your key responsibilities include: Lead and promote a ‘fit-for-purpose’ quality-focused culture within the ePID team, ensuring patient safety, security, data integrity, and privacy are always at the forefront Be the key architect of the ePID team’s Quality roadmap and implementation of it together with key stakeholders like test and release management Ensure quality implementation is based on best practice, and that activities are in sync with ongoing development and operations actions together with product management Drive planned quality improvement initiatives that are prioritised and follow up on their effect and relevance Provide hands-on Quality related subject matter expert (SME) support for ePID Product Management and ePID team members to develop and optimise quality-related processes, including the use of external partners to meet business challenges and regulatory requirements Align across the organization with for instance Good Clinical Practice Quality Assurance on estalishing and evaluation of quality monitoring and implementation of improvements both in terms of tools and processes Qualifications
To thrive and succeed, we expect you to have: Master’s degree in a relevant field such as Life Science, Engineering, Business, IT, or other. 3+ years’ experience working with quality processes, frameworks, and regulatory interactions and requirements from a quality assurance, product owner, or other relevant roles within the pharma industry Proven track in process improvement and project management Background in the digital domain and/or agile methodologies applied to digital product development would be a great asset but not a pre-requisite Proficient in written and spoken English As a person, you can work collaboratively with cross-functional teams to optimize quality-related processes. Your ability to adapt to evolving business goals and needs ensures alignment for product actions, making you a dynamic and indispensable contributor to our team. Furthermore, you consistently seek opportunities to enhance processes and strive for continuous improvement. About the department
You will join ePID team which is part of Clinical Digital Innovation in CVP area Clinical Drug Development Digital Transformation. Our vision is to provide easy trial setup, participation, and execution thereby supporting timely and accurate trial data collection. Our team is a diverse and collaborative group, harnessing a wide range of skills and expertise. We work closely with trial teams to ensure ePID is always functioning as intended. We work according to agile principles, adapting ePID quickly to business needs. In Clinical Drug Development Digital Transformation, we lead the digitalisation of clinical development to bring more innovative medicine to more patients faster. We drive the discovery and development of a portfolio of digital products ranging from large clinical trial management systems over data insights products to electronic Clinical Outcome Assessment (eCOA) solutions. Our portfolio consists of both solutions we built in-house as well as solutions from vendors. We have a razor-sharp focus on digital product management and product design to ensure that the products we create are desirable, feasible, and viable.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
If you want to know more about the position, you are very welcome to contact Martin Thuesen, Senior Director ePID at +45-34486994.
Deadline
9 November 2023. We will review applications on an ongoing basis, so we encourage you to apply as soon as possible.
To ensure a fair and efficient recruitment process, please refrain from adding a photo to your CV or resume. 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.
To thrive and succeed, we expect you to have: Master’s degree in a relevant field such as Life Science, Engineering, Business, IT, or other.
You will join ePID team which is part of Clinical Digital Innovation in CVP area Clinical Drug Development Digital Transformation. Our vision is to provide easy trial setup, participation, and execution thereby supporting timely and accurate trial data collection. Our team is a diverse and collaborative group, harnessing a wide range of skills and expertise. We work closely with trial teams to ensure ePID is always functioning as intended. We work according to agile principles, adapting ePID quickly to business needs. In Clinical Drug Development Digital Transformation, we lead the digitalisation of clinical development to bring more innovative medicine to more patients faster. We drive the discovery and development of a portfolio of digital products ranging from large clinical trial management systems over data insights products to electronic Clinical Outcome Assessment (eCOA) solutions. Our portfolio consists of both solutions we built in-house as well as solutions from vendors. We have a razor-sharp focus on digital product management and product design to ensure that the products we create are desirable, feasible, and viable.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
If you want to know more about the position, you are very welcome to contact Martin Thuesen, Senior Director ePID at +45-34486994.
Deadline
9 November 2023. We will review applications on an ongoing basis, so we encourage you to apply as soon as possible.
To ensure a fair and efficient recruitment process, please refrain from adding a photo to your CV or resume. 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 25.10.2023, 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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