ph3Associate Consultant Drug Safety /h3 pbLocation /b: Hybrid - Madridbr/bType /b: Full-time /p pThe QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offersknowledgetailored (software) solutionsin development, clinical, regulatory compliance, production and distribution for companies active inATMP, 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. /p h3What’s in it for you? /h3 pbMake a real impact: /b Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices /p pbGrow within a community of experts: /bBenefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise. /p pbBuild a meaningful career: /bAs an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences. /p pbA fair, competitive package: /b We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.br/ /p h3What you’ll be doing /h3 pGeneral Responsibilities: /p ul lipThe performance of tasks and duties of instrumental and highly predictable content in accordance with previously established instructions according to the rules, guidelines or ordinary procedures in regular use in the company, tasks for which they have the direct supervision of the immediate superior. /p /li lipEvery staff member of the Pharmacovigilance Department should be trained in each applicable SOP and WI according to general procedure /p /li lipDepending on the projects,



specific training in applicable client’s SOPs is also mandatory. /p /li /ul pSpecific responsibilities: /p ul lipCases management control /p /li lipData entry and quality control of PV cases in post-marketing and clinical trials, or related to medicinal products, medical devices and cosmetics. /p /li lipPV Assessment of any case of suspected adverse reaction. /p /li lipDirect contact with HCP and patients/consumers. /p /li lipPerform any follow up activities required. /p /li lipSubmission of cases to Eudravigilance, MHRA or any other Competent Authority. /p /li lipPerform bibliographic searches in local scientific journals, international journals, MLM service and any other type of search. /p /li lipManagement of medical information and answer of queries. /p /li lipReview and control of Safety Regulatory intelligence /p /li lipReview and control of Pharmacovigilance quality system /p /li lipParticipation in specific events related to their area of work. /p /li /ul h3What you bring /h3 pEducation: /p ul lipBachelor's degree in Life Sciences or related /p /li lipMaster's degree in Pharmacovigilance, Pharmaceutical Industry or related. Desirable. /p /li /ul pExperience: /p pWork experience as Trainee or Junior within pharmacovigilance and updated knowledge in Quality Assurance for the Pharmaceutical Industry is a plus. /p ul lipBibliographic search and database management.



Desirable /p /li lipKnowledge of European Good Pharmacovigilance Practices (GVPs). /p /li lipKnowledge regarding Eudravigilance requirements for Marketing Authorization /p /li lipHolders (clients) and the processes with the Health Competent Authorities. Desirable /p /li /ul pLanguages: /p ul lipHigh level of English. Must. /p /li lipProficient level of German. Must. /p /li /ul pOther: /p ul lipGood teamwork skills and high learning capacity is considered a plus. /p /li lipParticipative and proactive in work groups. /p /li lipAttention to detail /p /li lipSkills and/or experience in the writing of scientific texts. Desirable /p /li lipOrganization ability and task prioritization. /p /li /ul h3Who you are /h3 pOur culture is driven by values If this sounds like you, you’ll fit right in: /p ul lipYou’re bresilient /b and tackle challenges with a positive mindset /p /li lipYou’re bcurious /b and always up for learning something new /p /li lipYou have a bno non-sense approach /b honest, clear, respectful /p /li lipYou’re binnovative /b and bring ideas, not just opinions /p /li lipAnd above all, you’re bserious about your work, but not too serious about yourself /b /p /li /ul h3About us /h3 pWe 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. /p pWe believe in bJPEG /b: bJoy. Partnership. Going the Extra Mile. Getting Things Done. /b /p pYou 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

📌 Consultant Drug Safety - German (Pozuelo de Alarcón)
🏢 TRIUM Clinical Consulting
📍 Pozuelo de Alarcón