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From the employer's careers site First seen 27 Oct 2026

Study Monitor - In Vivo Toxicologist

ICON Strategic Solutions Remote senior contract

The employer hasn't listed a salary.

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Description

We are seeking an experienced toxicology professional to work as a Study Monitor for an in vivo toxicology study. As a Study Monitor, you will oversee toxicology and safety studies conducted through CRO partners, supporting study design, execution, oversight, and reporting.

Key Responsibilities:

  • Lead oversight of outsourced toxicology and safety studies
  • Partner with Project Toxicologists, CRO Study Directors, and cross-functional teams to deliver high-quality regulatory studies
  • Act as the primary point of contact for CROs throughout the study lifecycle
  • Support study design, execution, reporting, and communication of results to project teams
  • Ensure studies are delivered to agreed quality standards and timelines
  • Provide leadership and guidance to study monitors and key stakeholders
  • Participate in occasional study-related site visits as required

Requirements:

  • BSc or MSc in Toxicology, Pharmacology, or a related Life Sciences discipline
  • Experience in non-clinical safety assessment within the pharmaceutical, biotechnology, or CRO industry
  • Hands-on experience as a GLP Study Director and/or Study Monitor supporting in vivo toxicology studies
  • Strong understanding of toxicology and pharmacology principles
  • Knowledge of regulatory requirements governing non-clinical toxicology studies
  • Excellent communication, stakeholder management, and project coordination skills
  • Ability to influence and collaborate with internal and external partners at all levels

Preferred Experience:

  • Broad knowledge of regulatory toxicology study types across multiple species, delivery routes, and therapeutic modalities
  • Experience managing outsourced studies and CRO relationships

What We Offer:

  • Competitive base salary and performance-related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Skills

Required

  • Toxicology
  • Pharmacology
  • GLP Study Director
  • Study Monitor
  • Regulatory Toxicology

Nice to have

  • Regulatory Toxicology Study Types
  • CRO Relationships

Ready to apply?

You apply with the employer directly. Their original posting is here: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Project-Manager_JR161823

Apply on ICON Strategic Solutions