Who Collaborating Centre For Int Drug Monitoring jobb

Help shape the future of pharmacovigilance science Use your expertise in epidemiology to promote the safer use of medicines and vaccines worldwide. UMC is looking for a Senior Epidemiologist to join our Pharmacovigilance Science section and strengthen our research into medicines safety using global safety and healthcare data. Since 1978, Uppsala Monitoring Centre (UMC) has been dedicated to developing, supporting, and expanding the field of pharmacovigilance science and practice.  As a World Health Organization (WHO) Collaborating Centre, we support work around the world to examine the potential adverse effects of medicines and vaccines and contribute to safer, more informed care of patients.  We are a diverse, international group of pharmacists, physicians, data scientists, system developers, communicators, and many other professionals motivated by a deep belief that the work we do matters. About the role As a Senior Epidemiologist, you will contribute epidemiologicalexpertiseto our research and scientific development activities. Working at the intersection of epidemiology, pharmacovigilance, and real-world data, and with VigiBase, the WHO global database of adverse event reports, as well as other healthcare databases and registries, you will design, conduct, and interpret studies that strengthen our understanding of medicine safety and support evidence-based decision-making. This is a hands-on role spanning the full research process, from study design and data management to statistical programming, analysis, and scientific reporting. Working closely with colleagues across disciplines, you will help generate evidence that advances the science and practice of pharmacovigilance. You will join an international research environment dedicated to advancing the science of pharmacovigilance and improving the safer use of medicines globally. What you will do Lead and contribute to research aimed at improving the understanding and use of VigiBase, the WHO global database of adverse event reports, other healthcare databases, and health registries. Design epidemiological studies andprovidemethodological advice on study design and analytical approaches. Write,maintain, and review analytical code for the management and analysis of complex real-world data. Support signal management activities through data extraction, analysis, interpretation, and investigation of potential safety issues. Collaborate on multidisciplinary research projects using adverse event reporting and healthcare data. Contribute scientificexpertiseto research and methodological development in pharmacovigilance. Work closely with colleagues across Research, Signal Management, and other teams throughout the organisation. Who you are You havea strong foundationin epidemiological methods and enjoy working with complex real-world data. You are equally comfortable discussing study design with colleagues and writing the code needed to implement it. You combine scientificrigourwith practical judgement and enjoy collaborating across disciplines to deliver impactful research. You thrive in a collaborative, learning-oriented environment. You take responsibility for your work and shared team outcomes, are comfortable with uncertainty and complexity, and remain focused when managing multiple priorities. You value openness, learning, and different perspectives, and contribute to an environment of trust and psychological safety. Required An MSc or higher in epidemiology, public health, biostatistics, medicine, or a closely related field. At least two years' experience conducting observational epidemiological studies using complex real-world data, preferably including Swedish register data and/or individual case safety report data. Strongexpertisein causal inference, including identifying sources of bias and applyingappropriate analyticalmethods. A demonstrated record of scientific output, such as peer-reviewed publications or technical reports. Experienceprovidingmethodological guidance on study design, execution, and interpretation. Demonstrated experience programming and conducting epidemiological analyses using R and/or SQL (or another statistical programming language). Excellent written and spoken English. Desired qualifications A PhD in epidemiology, pharmacoepidemiology, public health, biostatistics, ora relateddiscipline. Experience in pharmacovigilance, drug safety, regulatory science, or post-marketing surveillance. Experience using Git for collaborative code management. Experience collaborating with international stakeholders. Experience mentoring junior scientists or contributing to scientific capacity building. Uppsala Monitoring Centre (UMC) is an independent, self-funded, non-profit foundation established in 1978 dedicated to safer use of medicines and vaccines. Through an agreement between the Government of Sweden and the World Health Organization (WHO), UMC operates the Programme for International Drug Monitoring, supporting over 180 member countries and regions in strengthening safety surveillance, and maintains VigiBase, the WHO global database of adverse event reports. In addition, UMC provides international standards and related digital solutions for secure exchange of pharmacovigilance data, including a global medicine and vaccine terminology for identification of medicinal products. With around 200 staff, UMC advances the science of pharmacovigilance and transforms its practice through technological innovation. UMC’s working language is English. We normally apply a probationary period to new appointments. If you have any questions regarding this position please contact the responsible manager. You will find the contact details at the end of this page. UMC follows the collective agreements between the Swedish Agency for Government Employers and Saco-S and ST. Union representatives are Malin Zaar (Saco-S) and Jessica Avasol (ST), +46 (0)18-65 60 60.

Would you like to contribute to the safe use of medicines and vaccines globally? We are looking for two Learning & Development specialists to join our Learning & Development section. Since 1978, Uppsala Monitoring Centre (UMC) has been dedicated to developing, supporting, and expanding the field of pharmacovigilance science and practice. As a World Health Organization (WHO) Collaborating Centre, we support work around the world to examine the potential adverse effects of medicines and vaccines and contribute to safer, more informed care of patients. We are a diverse, international group of pharmacists, physicians, data scientists, system developers, communicators, and many other professionals motivated by a deep belief that the work we do matters. About the role The Learning & Development section is part of UMC’s Communications & Learning department and is responsible for designing and developing online courses and overarching learning concepts. The section develops frameworks and structures to ensure alignment, continuous maintenance, and evaluation of learning initiatives. Through our Learning Management System (LMS), we offer courses designed for both a broad global audience and specific groups, including members of the WHO Programme for International Drug Monitoring (WHO PIDM) and users of UMC products. We are seeking someone who can translate complex information into clear, engaging, and accessible learning content. You are skilled in digital learning tools, instructional design principles, and LMS management, and you bring both structure and creativity to your work. You have the ability to develop training concepts and learning paths grounded in the needs expressed by the business areas. With a collaborative mindset and strong organisational skills, you confidently manage multiple learning initiatives at the same time. You are also comfortable presenting and facilitating workshops. You will report to the Head of Learning & Development section. What you will do - Design and develop online learning modules based on best practices in instructional design and adult learning theories - Administer and manage the LMS, including uploading courses, tracking progress and generating reports - Provide technical support for online learning throughout course life cycles - Collaborate with subject matter experts (SMEs) when developing learning content - Apply instructional design principles to ensure learning content is pedagogically sound, engaging, and aligned with organisational goals - Develop and deliver standardised presentations and learning materials for cross-functional use - Deliver and facilitate organisation-wide face-to-face workshops and courses Who you are - University degree in instructional design, educational technology or similar - A background in the life sciences, healthcare or similar is a plus - Creative with strong ability to translate complex information into clear and engaging learning content - Skilled in using Articulate 360 or similar e-learning authoring tools - Skilled in applying instructional design principles - Basic graphic design skills or familiarity with tools like Photoshop or Canva are an advantage - Experienced with LMS administration - Structured, organized, and able to manage multiple learning initiatives simultaneously - Collaborative and confident working with SMEs - Solution-oriented with the ability to turn needs into concrete learning experiences and training concepts. - Comfortable presenting and facilitating workshops for diverse audiences - Fluent in written and spoken English - Additional language skills are a plus Uppsala Monitoring Centre (UMC) is an independent, self-funded, non-profit foundation established in 1978 dedicated to safer use of medicines and vaccines. Through an agreement between the Government of Sweden and the World Health Organization (WHO), UMC operates the Programme for International Drug Monitoring, supporting over 180 member countries and regions in strengthening safety surveillance, and maintains VigiBase, the WHO global database of adverse event reports. In addition, UMC provides international standards and related digital solutions for secure exchange of pharmacovigilance data, including a global medicine and vaccine terminology for identification of medicinal products. With around 200 staff, UMC advances the science of pharmacovigilance and transforms its practice through technological innovation. UMC’s working language is English. We normally apply a probationary period to new appointments. If you have any questions regarding this position please contact the responsible manager. You will find the contact details at the end of this page. UMC follows the collective agreements between the Swedish Agency for Government Employers and Saco-S and ST. Union representatives are Malin Zaar (Saco-S) and Jessica Avasol (ST), +46 (0)18-65 60 60.