Drug Safety TraineeLocation: Hybrid - MadridType: Full-timeThe 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.What’s in it for you?Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devicesGrow within a community of experts:Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.Build a meaningful career:As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.What you’ll be doingGeneral Responsibilities:- To join the Collaborating Entity on the agreed date.- Comply with the timetable and respect its rules of operation,



safety and occupational risk prevention.- Comply 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).- If 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.- Maintain absolute confidentiality regarding all information to which they may have access because of the internship.Specific responsibilities:- Case management (data entry, control of pharmacovigilance cases in post-marketing and/or clinical trials, or related to medicinal, health and cosmetic products).- Contact with HCP and patients/consumers (for follow-up information).- Handling medical information and responding to any complaints.- Support in local and international literature search activities.- Support in authority search activities.- Support in website/social media monitoring.- Support in reconciliation activities.- Support in any other type of departmental activity.- Teamwork, both with people from the PV department and with colleagues from IM, Regulatory Affairs and Clinical Trials.What you bringEducation- Bachelor's degree in Life Sciences or related- Master's degree in Pharmacovigilance,



Pharmaceutical Industry or related. Desirable.ExperienceNo experience needed. Demonstrable interest in the pharmaceutical industry and pharmacovigilance.Skills and CompetencesLanguages:- High level of English. DesirableComputer:- Advanced informatic skills- Knowledge of MS Office. Desirable.Personal:- Good teamwork skills and high learning capacity is considered a plus.- Participative and proactive in work groups.- Attention to detail- Skills and/or experience in the writing of scientific texts. Desirable- Organization ability and task prioritization.Who you areOur culture is driven by values If this sounds like you, you’ll fit right in:- You’re resilient and tackle challenges with a positive mindset- You’re curious and always up for learning something new- You have a no non-sense approach honest, clear, respectful- You’re innovative and bring ideas, not just opinions- And above all, you’re serious about your work, but not too serious about yourselfAbout usWe 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.We believe in JPEG:Joy. Partnership. Going the Extra Mile. Getting Things Done.You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.#J-18808-Ljbffr

📌 Drug Safety Trainee (Madrid)
🏢 TRIUM Clinical Consulting
📍 Madrid