Associate Clinical Safety Professional (Parental leave cover - 12 months)

R&D Global Patient SafetySøborg, DenmarkThis is an extraordinary opportunity to apply your medical knowledge directly to the safety and quality of cutting-edge clinical development products, playing a pivotal role in global regulatory compliance. You’ll handle serious adverse events from clinical trials, making a tangible impact on patient safety while advancing your career in a highly regulated, dynamic environment.Your new roleAs an Associate Clinical Safety Professional, you will play a key role in handling serious adverse events reported from our clinical trials to ensure that global regulatory requirements are met.Your main responsibilities will include: Handle serious adverse events in the Veeva safety database and ensure sure that the reports are accurately and consistently registered and evaluated Assess the reports including need of requesting missing information on the reported events Take part in the conduct of clinical trials. Here you will maintain overview of individual adverse event reports in a specific clinical trial Be responsible for communication to relevant stakeholders regarding specific safety issues and other relevant information Cross functional collaboration and internal communication will therefore be a part of your everyday work Assist with related administrative and procedural activities and ensure that all tasks are performed in compliance with GxP requirementsYour new departmentSafety Operations Case Management Department is part of Safety Operations and one of the operational areas in Global Patient Safety. Global Patient Safety is responsible for meeting global regulatory requirements for handling and reporting of adverse events. Our department consists of three Case Management teams, each with 13 highly engaged colleagues.Your Skills And QualificationsWe are looking for a candidate who has the following qualifications: B.Sc. degree or M.Sc. degree, registered nurse or equivalent within health science Experience working in clinical setting Experience with clinical trials or pharmacovigilance (experience within the fields of diabetes, cardiology or obesity is an advantage) Experience using Veeva Safety Database or other Veeva modules Extensive knowledge of medicinal terminology and clinical pharmacology Interest in and flair for using IT-systems and strong skills in MS Office Proficiency in both written and spoken English is a requirement, as you will be working with international stakeholdersWith regards to personal skills, you are known for your good analytical skills and ability to collaborate. You are detail-oriented, diligent and have strong communication skills. In addition, this role will support the Safety team during a period of transition as we implement a new safety database over the next year, hence you will have to be adaptive to change.Working at Novo NordiskNovo 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 diverselife 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.What we offer In addition to a unique and supportive culture, Novo Nordisk offers strong learning and development opportunities tailored to your career and life stage. Our benefits reflect our commitment to empowering employees to reach their full potential while achieving work-life balance.More information For more information, please contact or Martin Duus Holle at DHOE@novonordisk.com or Marie Werngreen at MRWG@novonordisk.com.Deadline28 November 2025You do not need to attach a cover letter to your application, but please include a few sentences on your motivation for applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV.Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.