Junior Drug Safety Officer (Vet Profile)

TRIUM Clinical Consulting NV; Pozuelo de Alarcón; Presencial; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

A leading company in life sciences is seeking a Junior Drug Safety Officer. The role involves managing pharmacovigilance cases, assessing adverse reactions, and maintaining communication with healthcare professionals. Candidates should have a relevant degree and strong teamwork skills. Enjoy a supportive environment with opportunities for career growth and continuous learning.

Servicios

Attractive salary package

Career growth and job security

Continuous learning and development

Global success story participation

Formación

• Bachelor's degree required, Master's in Pharmacovigilance preferred.
• High proficiency in English and advanced IT skills desired.

Responsabilidades

• Manage case control and data entry for PV cases.
• Assess suspected adverse reactions and maintain contact with HCPs.
• Submit cases to Eudravigilance and conduct bibliographic searches.

Conocimientos

Teamwork

Learning Capacity

Scientific Writing

Organizational Ability

Educación

Bachelor's degree in Life Sciences

Master's degree in Pharmacovigilance

Herramientas

MS Office

Descripción del empleo

QbD Groupteam offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices / IVD. We are always looking for the next QbD’er in Pharmacovigilance.

What do we expect from you as a Junior Drug Safety Officer?

Employees in this role perform clearly established functions, with specific instructions and a high degree of organizational dependence.

The general responsibilities include:

1. Performing tasks with predictable content according to established instructions, rules, guidelines, or procedures under direct supervision.
2. Managing case control.
3. Data entry and quality control of PV cases in post-marketing and clinical trials related to medicinal products, medical devices, and cosmetics.
4. Assessing suspected adverse reactions.
5. Maintaining direct contact with HCPs and patients/consumers.
6. Following up on activities as required.
7. Submitting cases to Eudravigilance, MHRA, or other authorities.
8. Conducting bibliographic searches in scientific journals and databases.
9. Managing medical information and responding to queries.
10. Reviewing and controlling safety regulatory intelligence and PV quality systems.
11. Participating in relevant events related to the area of work.

Who are we looking for?

• Bachelor's degree in Life Sciences or related field.
• Master's degree in Pharmacovigilance, Pharmaceutical Industry, or related (desirable).
• High proficiency in English (desirable).
• Advanced IT skills.
• Knowledge of MS Office (desirable).

Personal skills:

• Good teamwork skills and high learning capacity.
• Participative and proactive attitude.
• Skills or experience in scientific writing (desirable).
• Organizational ability and task prioritization.
• Experience with bibliographic searches (desirable).
• Experience in Quality Assurance for the pharmaceutical industry (plus).
• Knowledge of European GVPs and Eudravigilance requirements.

Qualities of a true QbD’er:

• Resilient: positive attitude to overcome challenges.
• Hungry for knowledge: eager to learn.
• No-nonsense, respectful straightforwardness.
• Innovative: seeking new and better solutions.
• Balanced: professional yet approachable.

What’s in it for you?

• Attractive, tailored salary package.
• Career growth with job security and meaningful connections.
• Continuous learning and development.
• Be part of a global, award-winning success story.

Our promise to you:

• A supportive environment for thriving in life sciences.
• A joyful community fostering authenticity and growth.
• Our motto: JPEG — Joy in Partnership, going the extra mile to get things done!

Interested? Send your CV and motivation letter — maybe soon you'll join our QbD family!