🔍 Drug Safety Trainee - French

📍 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

Employees 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.

Main 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.

Main 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

Studies required:

• University degree in Pharmacy, Medicine or any branch of Health/Life Sciences.

• Postgraduate degree related to the pharmaceutical industry optional.

Required skills:

• High spoken and written level of English and French.

• Desirable ability to work in a team and social and communication skills.

• Desirable analytical and detail-oriented skills.

• Knowledge of MS Office desirable.

• Demonstrable interest in the pharmaceutical industry and pharmacovigilance.

Skills to develop:

• Acquire broad theoretical knowledge in PHARMACOVIGILANCE.

• Acquire practical experience and experience in teamwork and cooperation with other professionals in a multidisciplinary environment.

• Achieve optimal levels of interpersonal and organizational understanding.

• The internship plan will allow the student to integrate and get to know in detail the professional work within the biopharmaceutical sector.

🫵 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.