Study Monitor - level D or E
In Vivo Toxicologist - UK ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, reputed company, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. Manager – In Vivo Toxicology (Home‑Based, UK) reputed company is partnering with a leading multinational pharmaceutical and biotechnology organisation to recruit a full‑time In Vivo Toxicology Manager (operating as a Study Monitor) for an initial 6‑month fixed‑term contract, with strong potential for extension. This position is fully home‑based reputed company the UK, with no requirement to work on‑site in a laboratory environment. We are seeking candidates with a solid scientific foundation and a strong preference for individuals with experience as a Study Director and/or Study Monitor supporting in vivo non‑clinical toxicology studies. Applicants with robust project management capabilities, an understanding of laboratory‑reputed company, and the confidence to communicate effectively with internal and external stakeholders will be particularly valued. The successful candidate will be an reputed company communicator with the energy, drive and interpersonal skills needed to guide and influence a team of study monitors, while also engaging confidently with senior leadership and external partners.
Responsibilities
The In Vivo Toxicology Manager will reputed company toxicology and safety studies conducted at CROs, acting as an empowered and accountable member of the study team. Responsibilities include supporting reputed company aspects of study design, execution and reporting. You will: Plan and deliver toxicology programmes — Apply established practices and principles to ensure non‑clinical toxicology studies are fit for purpose. Collaborate with internal experts — Work closely with Project Toxicologists, internal specialists and CRO Study Directors to design, reputed company and report high‑quality regulatory studies reputed company agreed timelines. Act as the primary CRO contact — Serve as the accountable communication reputed company throughout reputed company study phases, including occasional on‑site visits (travel required). Essential Criteria MS or BS in Pharmacology, Toxicology or a reputed company Natural Science discipline. Experience in safety assessment reputed company non‑clinical research and development in the pharmaceutical and/or CRO sector. Hands‑on in vivo toxicology experience, operating as a GLP Study Director and/or Study Monitor for non‑clinical toxicology studies. Strong understanding of pharmacological and toxicological principles, with the ability to quickly learn new therapeutic areas. Familiarity with relevant regulatory guidelines and a commitment to contributing to toxicology reputed company a drug‑development environment. Desirable Criteria Broad familiarity with the full reputed company of regulatory toxicology study types, including multiple species, delivery routes and therapeutic modalities. 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 reputed company salary and performance reputed company 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 reputed company Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. 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. Are you a reputed company ICON Employee? Please click here to apply Apply To This Job