Drug Safety Trainee

Location: Hybrid - Madrid
Type: Full-time

The QbD Group supports life sciences companies worldwide from idea to patient. QbDs 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.

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.

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 Aziertas 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.

Education

- Bachelors degree in Life Sciences or related

- Masters 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.

Our culture is driven by values If this sounds like you youll fit right in:

• Youre resilient and tackle challenges with a positive mindset

• Youre curious and always up for learning something new

• You have a no non-sense approach honest clear respectful

• Youre innovative and bring ideas not just opinions

• And above all youre serious about your work but not too serious about yourself

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 wont just be taking a job youll be joining a community where people grow laugh build and contribute to something bigger.

Interested Lets talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family.