Senior Toxicologist

S3 Science Recruitment; Barcelona; Híbrido; EUR 166.000 - 221.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible setup: fully remote or on-site

Opportunity to contribute to a high-visibility international project

Descripción de la vacante

A recruitment agency is looking for an experienced Senior Toxicologist for a contract role in Spain. The successful candidate will provide scientific leadership and support for a high-visibility project, bringing over 12 years of expertise in toxicology and non-clinical safety. Opportunities are available for both remote and on-site work. Candidates should be proactive and able to work independently.

Formación

• Minimum 12 years’ professional experience in toxicology.
• Strong background in non-clinical safety assessment.
• Proven experience in study design, data interpretation, and strategy.
• Regulatory submission experience highly beneficial.

Responsabilidades

• Lead and advise on non-clinical toxicology strategy across development programs.
• Design, review, and interpret toxicology studies.
• Prepare or contribute to regulatory documentation.
• Support regulatory interactions as needed.
• Collaborate effectively with cross-functional teams.

Conocimientos

Toxicology expertise

Non-clinical safety assessment

Study design

Data interpretation

Regulatory submissions

Independent working

Descripción del empleo

Senior Toxicologist – Contract (Remote or On-Site, Spain)

Location: Spain (Remote or On-Site)

Contract Type: Freelance/Contract

Experience: 12+ years

Overview

Our client is initiating a major project in Spain and is seeking an experienced Senior Toxicologist to provide high-level scientific leadership on a contract basis. The ideal consultant will bring deep expertise in toxicology and non-clinical safety, supporting strategic input across complex development activities.

Key Responsibilities

• Lead and advise on non-clinical toxicology strategy across development programs
• Design, review, and interpret toxicology studies
• Prepare or contribute to regulatory documentation
• Support regulatory interactions as needed
• Collaborate effectively with cross-functional teams

Requirements

• Minimum 12 years’ professional experience in toxicology
• Strong background in non-clinical safety assessment
• Proven experience in study design, data interpretation, and strategy
• Regulatory submission experience highly beneficial
• Ability to work independently and proactively

What We Offer

• Flexible setup: fully remote or on-site in Spain
• Opportunity to contribute to a high-visibility international project