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.
* 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. Must. 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. #J-18808-Ljbffr

📌 Drug Safety Trainee (Comunidad de Madrid)
🏢 QbD Group
📍 Comunidad de Madrid