ph3Drug Safety Trainee - French /h3pLocation: Hybrid - Madridbr/Type: Full-time /ppThe QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge tailored (software) solutions in development, clinical, regulatory compliance, production and distribution for companies active in ATMP, Biotech, Medical Devices, In Vitro Diagnostics, Digital Health and Pharma.QbD has affiliates in 8 different countries and can count on the expertise of more than 500 life science professionals and growing. /ph3What’s in it for you? /h3pMake a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices /ppGrow within a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise. /ppBuild a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences. /ppA fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued. /ph3What you’ll be doing /h3pEmployees belonging to this professional category perform clearly established functions focused on the learning plan of the internship with specific instructions and a high degree of organizational dependence. /ppbMain general responsibilities /b /pullipTo join the Collaborating Entity on the agreed date. /p /lilipComply with the timetable and respect its rules of operation, safety and occupational risk prevention. /p /lilipComply with the training project following the instructions of the tutors (both Azierta's internal training and the training provided by the clients in the projects involved).



/p /lilipIf the student leaves the extracurricular internship before completing the period of time indicated in the Annex regulating external internships without a justified cause, he/she will not be able to apply for another extracurricular internship with the FLT Academy internship department. /p /lilipMaintain absolute confidentiality regarding all information to which they may have access because of the internship. /p /li /ulpbMain Specific responsibilities /b /pullipCase management (data entry, control of pharmacovigilance cases in post-marketing and/or clinical trials, or related to medicinal, health and cosmetic products). /p /lilipContact with HCP and patients/consumers (for follow-up information). /p /lilipHandling medical information and responding to any complaints. /p /lilipSupport in local and international literature search activities. /p /lilipSupport in authority search activities. /p /lilipSupport in website/social media monitoring. /p /lilipSupport in reconciliation activities. /p /lilipSupport in any other type of departmental activity. /p /lilipTeamwork, both with people from the PV department and with colleagues from IM, Regulatory Affairs and Clinical Trials. /p /li /ulh3What you bring /h3pbStudies required: /b /pullipUniversity degree in Pharmacy, Medicine or any branch of Health/Life Sciences. /p /lilipPostgraduate degree related to the pharmaceutical industry optional. /p /li /ulpbRequired skills: /b /pullipHigh spoken and written level of bEnglish and French.



/b /p /lilipDesirable ability to work in a team and social and communication skills. /p /lilipDesirable analytical and detail-oriented skills. /p /lilipKnowledge of MS Office desirable. /p /lilipDemonstrable interest in the pharmaceutical industry and pharmacovigilance. /p /li /ulpbSkills to develop: /b /pullipAcquire broad theoretical knowledge in PHARMACOVIGILANCE. /p /lilipAcquire practical experience and experience in teamwork and cooperation with other professionals in a multidisciplinary environment. /p /lilipAchieve optimal levels of interpersonal and organizational understanding. /p /lilipThe internship plan will allow the student to integrate and get to know in detail the professional work within the biopharmaceutical sector. /p /li /ulh3Who you are /h3pOur culture is driven by values If this sounds like you, you’ll fit right in: /pullipYou’re bresilient /b and tackle challenges with a positive mindset /p /lilipYou’re bcurious /b and always up for learning something new /p /lilipYou have a bno non-sense approach /b honest, clear, respectful /p /lilipYou’re binnovative /b and bring ideas, not just opinions /p /lilipAnd above all, you’re bserious about your work, but not too serious about yourself /b /p /li /ulh3About us /h3pWe support life sciences companies from idea to patient - offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma. /ppWe believe in bJPEG /b: br/bJoy. Partnership. Going the Extra Mile. Getting Things Done. /b /ppYou won’t just be taking a job - you’ll be joining a community where people grow, laugh, build, and contribute to something bigger. /p /p #J-18808-Ljbffr

📌 Drug Safety Trainee - French (Pozuelo de Alarcón)
🏢 TRIUM Clinical Consulting
📍 Pozuelo de Alarcón