Drug Safety Trainee
🔍 Drug Safety Trainee
đź“Ť Location: Hybrid - Madrid
đź•“ 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.
đź’Ş 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.
- Service
- Vigilance
- Role
- Drug Safety
- Locations
- QbD Spain (Madrid)
- Remote status
- Hybrid