Team Leader, Content Management Team
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Søborg
At Novo Nordisk, our commitment to improving patients' lives is unwavering. We invite you to step into a role where you can make a real difference as the Team Leader of our Content Management Team. In this dynamic position, you will have the opportunity to lead a talented team and support newly developed digital products. If you're ready to combine your leadership skills with your passion for innovation and scientific excellence, we encourage you to explore this exciting opportunity. Apply now for this life-changing job opportunity!
The position As the Team Lead of Content Management Team, you will be an integral part of supporting the operational implementation of one of our newly developed digital products NovoScribe, which has been developed to produce clinical study reports (CSRs). NovoScribe is an automated authoring platform developed using a structured authoring approach and natural language processing. It fosters a standardized, validated, and methodical approach to document creation. NovoScribe utilizes automated integration of statistical results by incorporating systematic tagging, topic-based authoring and enables reuse of standardized texts across trials. The aim of the product is to transform the way we write documents (e.g., clinical study reports) by introducing automation and natural language processing. You will be working in a transformative and innovative team, which is leading the pharmaceutical industry in automated document creation.
Your key responsibilities include: Leads team in line with Novo Nordisk way to ensure optimal employee development, planning and resource utilisation Responsible for people processes and people development including ongoing feedback on performance, job descriptions, Individual Development Plans (IDP) Managing the maintenance of the database and day-to-day running of the team Taking responsibility and ownership for upholding the highest standards of scientific accuracy, quality and compliance with all applicable industry guidelines, local and international Exercise excellent interpersonal/communication skills for effective and professional liaison with the internal team, clients, healthcare professionals and other key stakeholders and to obtain comprehensive briefs and responses to queries Effectively partner with customers to understand their business needs and how content creation will contribute to their success
Qualifications To be a successful candidate, you need to have a master’s degree within natural sciences (MSc., MSc. Pharm. or equivalent), preferably supplemented with a PhD and/or relevant experience in the pharmaceutical industry. You should also possess the following: Good understanding of pharmaceutical industry, clinical development, and regulatory processes The ability to identify better practice and create improvements in methods, techniques, and approaches Team supervision experience Business and R&D (Research & Development) value chain understanding Experience with a broad range of different medical writing tasks Practical knowledge of software development pipelines and experience in using and maintaining databases would be viewed as beneficial, although it is not obligatory
For this position, we seek an individual who has an exceptional interpersonal, communication, and presentation skills. Furthermore, we highly value strong mentoring and training abilities. The ideal candidate should excel in working seamlessly within cross-functional teams, including geographically diverse ones, while cultivating robust collaborative relationships. Their problem-solving skills should demonstrate clarity and logic, and they should exhibit ease in adapting to changing conditions. Moreover, we value pragmatism and a willingness to challenge the status quo. You will be expected to work independently with a positive and can-do attitude. Your ability to think through problems clearly and logically, coupled with your adaptability, will make you an asset to our team and help us drive forward in an ever-changing environment. About the department
You will join us in Clinical Reporting, the medical writing function at Novo Nordisk, currently comprising around 150 Medical Writers worldwide. We are part of Novo Nordisk Development and anchored in the Submission & Life Cycle Management area. Development is responsible for managing clinical drug development and submissions to health authorities worldwide, from the early development phases to market authorisation. Our supportive culture drives business transformation and we value continuous learning, being bold and striving for simplicity. Clinical Reporting covers all clinical drug development projects across therapy areas. Our main focus is to use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials and our main task is to communicate clinical data in a clear and concise manner.
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 For further information, please contact Louise Lind Skov, Head of Content Digitalisation, at +45 30755710. Deadline 21 September 2023. Note that relevant candidates may be invited for interviews on an ongoing basis before the deadline. 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. 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.
The position As the Team Lead of Content Management Team, you will be an integral part of supporting the operational implementation of one of our newly developed digital products NovoScribe, which has been developed to produce clinical study reports (CSRs). NovoScribe is an automated authoring platform developed using a structured authoring approach and natural language processing. It fosters a standardized, validated, and methodical approach to document creation. NovoScribe utilizes automated integration of statistical results by incorporating systematic tagging, topic-based authoring and enables reuse of standardized texts across trials. The aim of the product is to transform the way we write documents (e.g., clinical study reports) by introducing automation and natural language processing. You will be working in a transformative and innovative team, which is leading the pharmaceutical industry in automated document creation.
Your key responsibilities include:
Qualifications To be a successful candidate, you need to have a master’s degree within natural sciences (MSc., MSc. Pharm. or equivalent), preferably supplemented with a PhD and/or relevant experience in the pharmaceutical industry. You should also possess the following:
For this position, we seek an individual who has an exceptional interpersonal, communication, and presentation skills. Furthermore, we highly value strong mentoring and training abilities. The ideal candidate should excel in working seamlessly within cross-functional teams, including geographically diverse ones, while cultivating robust collaborative relationships. Their problem-solving skills should demonstrate clarity and logic, and they should exhibit ease in adapting to changing conditions. Moreover, we value pragmatism and a willingness to challenge the status quo. You will be expected to work independently with a positive and can-do attitude. Your ability to think through problems clearly and logically, coupled with your adaptability, will make you an asset to our team and help us drive forward in an ever-changing environment. About the department
You will join us in Clinical Reporting, the medical writing function at Novo Nordisk, currently comprising around 150 Medical Writers worldwide. We are part of Novo Nordisk Development and anchored in the Submission & Life Cycle Management area. Development is responsible for managing clinical drug development and submissions to health authorities worldwide, from the early development phases to market authorisation. Our supportive culture drives business transformation and we value continuous learning, being bold and striving for simplicity. Clinical Reporting covers all clinical drug development projects across therapy areas. Our main focus is to use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials and our main task is to communicate clinical data in a clear and concise manner.
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 For further information, please contact Louise Lind Skov, Head of Content Digitalisation, at +45 30755710. Deadline 21 September 2023. Note that relevant candidates may be invited for interviews on an ongoing basis before the deadline. 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. 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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 11.9.2023, 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.
- Forretningsudvikler
- Søborg
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