Data Manager

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Aalborg

Do you aspire to make a positive impact in global project teams, contributing to the discovery and development of innovative biological medicines and making them accessible to patients throughout the world? Are you intrigued by taking on the responsibility for collecting and processing data from global clinical trials within a world-class development organization? Our Data Management organization is growing, and we are looking to employ several data managers at all seniority levels. The positions will be based in our offices in either Søborg, Aalborg or Madrid. Apply now!

The position
The Trial Data Management department is expanding, and we are therefore offering several opportunities for data management positions at various levels of seniority. As a Data Manager at Novo Nordisk, you will be responsible for ensuring timely and high-quality data management deliverables for the clinical trials you are involved in. Your responsibilities will include:
  • Coordinating and executing data management activities through trial planning, set-up, execution, and closure
  • Supervising and evaluating the data management processes throughout the life cycle of a clinical project
  • Working closely with colleagues in our global Data Management organization, as well as being an integral part of the clinical trial team – stakeholder management is an important part of the role
  • Acting as the bridge between our many stakeholders and the data management colleagues involved in your clinical trials with a key focus on clear communication
    • For the experienced candidate we may also offer opportunities for responsibility for a larger portfolio of activities within the department.
    Being innovative and developing fit for purpose solutions, sharing your knowledge with peers and being an active partner in transformational activities is a key priority for Trial Data Management. This requires us to excel in our project leadership, our communication and it requires us to have a solid understanding of the data we collect in order to provide meaningful insights for our stakeholders. Qualifications
    We imagine our candidate having below:
  • At least a Bachelor’s degree in a relevant field, possibly within data science or natural sciences.
  • Excellent project leadership skills are required as you are expected to plan for and lead multiple activities in parallel without compromising the quality of your work, also when things are moving at a high pace
  • You are a skilled communicator and fluent in English, both written as well as spoken and you can explain complex, technical issues in a layman’s context. You work independently, take responsibility, and show initiative
  • Experience with the collection and processing of high volumes of complex data
    • For higher seniority-level positions:
  • Experience from the pharma industry, e.g., within data management, biostatistics or other data science functions working with clinical trial data is required
  • A solid understanding of GCP and relevant regulatory requirements is required
  • Experience working with industry-standard clinical data management systems (Inform, Rave, Data Management Workbench etc.), relational databases and data visualization tools

    • About the department
    Trial Data Management is part of the global Data Management organization within the Data Science area at Novo Nordisk. We are responsible for ensuring the integrity and timely flow of clinical trial data through the many systems we use for data collection for our clinical trials, conforming to regulatory requirements and industry-standards. Trial Data Management delivers high quality data for further analysis, reporting and submission and work with a wide range of stakeholders across the global Novo Nordisk organization.
    In Trial Data Management, we always strive for an inspiring working environment with focus on diversity, collaboration, and opportunities for personal growth for ambitious and motivated individuals. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.
    Contact For any futher information, please contact Anders Mikkel Harboe, Director +45-30797866
    Deadline
    18 February 2024. We will initiate candidate interviews prior to the deadline. You do not need to attach a cover letter to your application, but please describe your motivation 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 "Softwareudvikler", og befinder sig i kategorien "Informationsteknologi".

    Arbejdsstedet er beliggende i Aalborg

    Jobbet er oprettet på vores service den 29.1.2024, men kan have været deaktiveret og genaktiveret igen.

    Rapportér
    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Softwareudvikler
    • Aalborg
    Rapportér

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