Regulatory Affairs input to planned approvals of new Marketing Authorizations and line-extensions.Maintenance of established products and clinical trial applications.Translation of SmPCs, submission of DSUR and PSUR.Handling of Health Authority requests. Interaction with Marketing/Sales, Logistics and Clinical regarding products and Projects.

Handling Adverse Event Reports (AE) and performing follow-up, also for AEs from clinical trials, post-marketing studies and commercial programs in Scandinavia. Screening litterature, executing Risk Management Plan commitments, submitting reports to Health Authorities. Reconciling with other departments. Preparing/submitting KPI reports.Training colleagues in Adverse Event reporting. Liaising with Marketing and sales on Marketing Programs in Scandinavia.Drive and monitor local execution of Risk Management Plans (RMP) for all products: training of colleagues in RMP, support local execution of pharmacovigilance activities defined in RMP, liaising with Regulatory Affairs to ensure tracking of RMP commitments implemented locally, liaising with Marketing to ensure implementation of Educational Material.Deputize Drug Safety Responsible.

Temporary position. Working with the Danish Drug Interaction Database:Quality assurance. Evaluation of studies for updating the database and inclusion of the most important study information.Standardization of the database-content.Handling of user-inquiries.

Performance of in vivo studies.Handling of large quantities of data.Dataprocessing and presentation of data through GraphPad Prism.Statistical evaluation of data through Statview.Dissemination of data through a professional and clearly formulated scientific report.Oral presentation of scientific results to academics.

Student job.Sale of drugs. Needs analysis. Giving professional advice.Communication of information to the patients.Receiving prescriptions from doctors over the phone.Control of the dosage set by the doctor.

Full time job.Drug sale, needs analysis and professional advice.Identification of drug-related problems when performing medication reviews.Identification of the adverse effects of a drug, based on patient-conversations.Quality assurance of the database for registration of prescription-interventions. Education of pharmacy-staff by taping informationvideos.