Associate Consultant Drug Safety (Madrid)

Associate Consultant Drug Safety (Madrid)

12 ago
|
Qbd Group | Spain
|
Madrid

12 ago

Qbd Group | Spain

Madrid

Overview

The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge and 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 offer an environment to thrive in life sciences.
- A fair, competitive package: Transparent compensation aligned with expertise, preferences, and local market regulations.

Responsibilities





General responsibilities:
- The performance of tasks and duties of instrumental and highly predictable content in accordance with previously established instructions, rules, guidelines or ordinary procedures in regular use in the company, under direct supervision of the immediate supervisor.
- Every staff member of the Pharmacovigilance Department should be trained in each applicable SOP and WI according to general procedure.
- Depending on the projects, specific training in applicable client’s SOPs is also mandatory.

Specific responsibilities:
- Cases management control data entry and quality control of PV cases in post‑marketing and clinical trials, or related to medicinal products, medical devices and cosmetics.
- PV assessment of any case of suspected adverse reaction.
- Direct contact with HCP and patients/consumers.
- Perform any follow‑up activities required.
- Submission of cases to Eudravi

📌 Associate Consultant Drug Safety (Madrid)
🏢 Qbd Group | Spain
📍 Madrid

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