Time for change - time for a new job! Are you an Employee for Patient Safety looking for a new professional challenge? Then look no further! We have what you are looking for: a secure job, fair compensation and exciting new tasks at an attractive pharmaceutical company in Nürnberg.Das dürfen Sie erwartenThis position is remunerated above the standard pay scaleIncreasing salary with increasing length of service in companies in the chemical industry: up to 67% more basic salaryExtensive social benefits, incl. Christmas and holiday bonusesRepresentation of interests by a comprehensive works councilUse of the Randstad App (leave requests online, payroll viewable at any time and much more)Ihre AufgabenManage collection, processing, documentation, reporting and follow-up of all adverse event reports for all company products from non-interventional studies, Patient Oriented Programs, Spontaneous ReportsTranscribe, translate and enter data of all data from source documents into safety systems accurately and consistently with emphasis on timeliness and qualityWork with other local/global Patient Safety associates to ensure accurate evaluation of safety dataInteract and exchange relevant safety information with local HA, Patient Safety associates, other functional groups and third party contractor, if applicableInput, review and approval of program proposals for language, content and establishment of necessary controls on collection and reporting of adverse event informationPerform reconciliation with other departments (e.g. Medical Information, Quality Assurance and third party contractor, if applicable) for potential AEs resulting from medical inquiries, quality related complaints and other sourcesDevelop and update training materials for pharmacovigilance and ensure training of Country Organization associates on relevant Patient Safety procedures for AE reporting, including field force and third party contractor, if applicableManage and maintain efficient Patient Safety filing and archive systemUnsere AnforderungenCompleted education as a health care sciences professional (e.g. Medical Doctor, Nurse, Pharmacist) or natural scientist with experience in the area of pharmacovigilance and/or regulatory area and/or clinical developmentKnowledge of national and international regulations for pharmacovigilanceKnowledge of pharmacological and medical terminologyFluent in English and German (both written and spoken) Computer skillsExcellent communications, interpersonal and negotiation skillsQuality and focus oriented Unhappy with your job? We can offer you a good work-life balance. Sounds interesting? See what we can offer. Randstad is a trustworthy and technology-driven partner but at the same time very personal. We help companies and applicants realize their true potential. Because we know from experience that real connections do not arise from data and algorithms - they need human interaction, empathy and intuition.Corona virus and application at Randstad: Our application process supports our "Human Forward" promise. This currently means: Avoid personal contacts, because the health of our candidates and employees and our shared social responsibility have top priority for us. We enable you working conditions that take into account the currently necessary precautionary measures. Equipping with protective masks, maintaining safety distances, disinfection measures and, if necessary, COVID 19 tests are a matter of course for us. Therefore, our application process is still completely possible without direct and personal contact.If you are interested please apply online. Applications from severely disabled people are of course welcome. We are looking forward to meeting you.