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’reresilient and tackle challenges with a positive mindset

• You’recurious and always up for learning something new

• You have ano non-sense approach honest, clear, respectful

• You’reinnovative and bring ideas, not just opinions

• And above all, you’reserious 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 inJPEG:
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.