Project Manager

Study Monitor - In Vivo Toxicologist

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

Manager – In Vivo Toxicology (Home-Based, UK)

ICON Strategic Solutions is partnering with a leading global pharmaceutical and biotechnology organisation to recruit an In Vivo Toxicology Manager (operating as a Study Monitor) for an initial 6-month fixed-term contract, with strong potential for extension. This is a fully home-based UK role with no requirement to work within a laboratory environment.

We're seeking an experienced toxicology professional with a strong scientific background and proven experience supporting in vivo non-clinical toxicology studies as a Study Director, Study Monitor, or similar. You'll combine technical expertise with strong project management and stakeholder engagement skills to support the delivery of high-quality regulatory toxicology programmes.

The Role

As an accountable member of the study team, 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.

About You

• 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.

Why Apply?

This is an excellent opportunity to join a high-performing global team and play a key role in the delivery of critical non-clinical toxicology programmes, working with leading scientific experts while enjoying the flexibility of a fully home-based position.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• 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

Benefits may vary depending on role and location.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.