Are you ready to play a central role in how Novo Nordisk governs pharmacovigilance excellence across the globe? This is your chance to help shape the systems, processes and training frameworks that keep our pharmacovigilance operations compliant, inspection-ready and continuously improving – directly supporting patient safety at scale.
A masters degree and/or PhD in Life Sciences e.g. Pharmacy, Medicine, Veterinary, or Biological Sciences, combined with experience working within pharmacovigilance and medical writing
Bachelors or Masters degree in life sciences, natural sciences, engineering, or equivalent qualifications. 2-3 years of programming experience, preferably working with biological data or equivalent knowledge through relevant practical experience.
Looking for a Clinical Data Management Professional who thrives in a dynamic, international environment and brings a strong commitment to data quality and regulatory compliance.
Managing initial clinical trial application submissions in the EU according to the Clinical Trial Regulation and all changes during the life cycle of clinical trials.
Conduct medical review of all trial subjects in assigned clinical trials to ensure high-quality, consistent medical data. Ensure patient safety and adherence to protocols, Good Clinical Practice, ICH Guidelines, local regulations, and SOPs.
Bachelor degree in Pharma or Life Science. pharmaceutical sales experience, preferably with diabetes products. Consistent record of meeting or exceeding sales targets