Drug Safety Trainee

🔍 Drug Safety Trainee 📍 Location : Hybrid - Madrid 🕓 Type : Full-time The 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 devices Grow 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 doing General 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 bring Education - Bachelor's degree in Life Sciences or related - Master's degree in Pharmacovigilance, Pharmaceutical Industry or related. Desirable. Experience No experience needed. Demonstrable interest in the pharmaceutical industry and pharmacovigilance. Skills and Competences Languages: - High level of English. Desirable Computer: - 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 are Our 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 yourself ✨ About us We 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. 📩 Interested? Let’s talk. Send us your CV and motivation letter. You could be the next one to join the QbD family.