Data Manager
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Do you enjoy working with Clinical Data? Do you thrive in ensuring data accuracy and compliance? Want to make a meaningful impact on patient care? If you have meticulous attention to detail, organizational skills, and a desire to drive medical advancements, we want you! Take the next step in your career and join our team as a Data Manager. Apply now! The position As a Data Manager, you will be accountable for project management and end-to-end trial delivery from data management. Being a standing member of the Trial Squad that drives clinical trials you will be accountable for Data Management ( DM) related project risk identification, issue prevention and resolution, decision facilitation and management reporting. In addition, your responsibilities will include: End-to-end trial delivery from Data Management in accordance with project goals, plans and assigned activities
Participate in and provide inputs to protocol outline and protocol development
Set up databases
Define data collection structure and specifications in collaboration with internal and external stakeholders
Create, maintain and execute a Data Management Plans covering all DM activities
As part of your role, you will initiate contact with relevant internal and/or external stakeholders to secure the best possible scientific cooperation and results across functions and teams. Stakeholders will include, but not be limited to, Trial Management, Data Standards, Biostatistics and CROs. Qualifications To succeed in this role, you have: A MSc or BSc degree within data science, Natural or Tech Sciences, or other relevant degree
It would be an advantage if you have: Practical experience from working with clinical data and systems used in drug development
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
Background with the collection and processing of high volumes of complex data
Experience working with industry-standard clinical data management systems (Inform, Rave, Data Management Workbench etc.), relational databases and data visualisation tools
Strong communication skills and fluency 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
Solid understanding of Good Clinical Practice (GCP) and relevant regulatory requirements
Knowledge of programming languages such as Python would be considered a plus but is not a requirement. As a person you are team oriented with a high degree of flexibility, situational- and cross-cultural awareness. With strong communication skills you are able to translate complex and technical information to different stakeholders. You can build and maintain a strong network; your people skills make you an adaptable and trustworthy co-worker. About the department Trial Data Management Phase 1 & NIS is part of the global Data Management & Centralised Data Review (DMCDR) organisation 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 organisation. In DMCDR, 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 further information, please contact Director Thomas P. See (+45 3079 6364). Deadline 5 November 2023. 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 "Softwareudvikler", og befinder sig i kategorien "Informationsteknologi".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 16.10.2023, 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.
- Softwareudvikler
- Søborg
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