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. What ICON Can Offer You Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include
• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.