# Study Monitor - In Vivo Toxicologist

**Company**: ICON Strategic Solutions
**Work arrangement**: remote
**Experience**: senior
**Job type**: contract
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Project-Manager_JR161823?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_4a695290-755

## 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

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Project-Manager_JR161823?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)