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ICON plc is a world-leading healthcare intelligence and clinical research organization. A Senior Global Project Manager will lead and manage global projects, ensuring successful execution and delivery of objectives. Responsibilities include developing project plans, leading cross-functional teams, and stakeholder collaboration. The role requires oncology project management experience, strong leadership, and the ability to manage budgets, vendor oversight, and travel (approx. 25%). #J-18808-Ljbffr

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Pharmacologist (Director, Clinical Pharmacology) to join our growing client-dedicated team at ICON. This is a unique opportunity to become an embedded strategic partner within a leading global pharmaceutical organization, influencing development programs from early research through registration. As a Senior Clinical Pharmacologist, you will join a highly collaborative client-dedicated team, partnering with scientific and clinical leaders to support clinical pharmacology strategy across programs from early development through registration. You will apply your expertise in clinical pharmacology, biopharmaceutics, and model-informed drug development to drive informed decision-making and accelerate the development of innovative therapies. • Lead clinical pharmacology strategies across early and late-phase drug development programs., • Apply model-informed drug development principles to support dose selection, patient population strategy, biomarkers, and endpoint optimization., • Partner with Pharmacometricians to develop and execute PK/PD modeling and simulation strategies., • Contribute to translational medicine initiatives, preclinical study design, and First-in-Human (FIH) studies, including SAD and MAD dose selection., • Provide clinical pharmacology expertise to cross-functional teams, governance discussions, and key development decision points., • Support regulatory submissions and responses to health authority queries., • Drive collaboration across preclinical, clinical, regulatory, and quantitative sciences teams to advance development programs., • Stay current with emerging innovations in clinical pharmacology, pharmacokinetics, biopharmaceutics, and quantitative drug development., • PhD in Biological Sciences, Bioengineering, Pharmacology, Pharmaceutical Sciences, or a related discipline., • Extensive experience within clinical pharmacology, pharmaceutical development, or a related industry setting., • Strong hands-on expertise in clinical pharmacology strategy, study design, PK/PD modelling, and quantitative data interpretation., • Deep understanding of model-informed drug development and its application across the drug development lifecycle., • Experience supporting translational medicine strategies and early clinical development programs, including FIH studies., • Strong knowledge of innovative approaches in clinical pharmacokinetics, biopharmaceutics, and PK/PD modelling., • Comprehensive understanding of global drug development and regulatory requirements., • Excellent communication and stakeholder management skills, with the ability to influence and build alignment across scientific and business functions., • Proven ability to lead complex scientific discussions and contribute to strategic development decisions. 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’s well-being. • 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. #J-18808-Ljbffr

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Senior Director, Biometrics within ICON Strategic Solutions, you will provide strategic leadership across biometrics delivery for a dedicated client partnership. Acting as a trusted advisor to senior client stakeholders, you will ensure the successful execution of biometrics activities while driving operational excellence, quality, and delivery performance across global clinical development programs. • Providing strategic leadership and governance across biometrics delivery, ensuring quality, efficiency, and regulatory compliance., • Building and maintaining strong partnerships with senior client stakeholders, serving as the primary biometrics escalation point and trusted advisor., • Collaborating with client and internal leadership teams to align biometrics strategy with business objectives, clinical development priorities, and future portfolio needs., • Driving operational excellence through effective oversight of delivery performance, resource planning, risk management, and quality metrics., • Leading global, cross-functional teams to ensure successful execution and consistent delivery across complex clinical programs., • Supporting long‑term account success through proactive planning, continuous improvement initiatives, and identification of opportunities to enhance client value and operational effectiveness., • Championing innovation and best practices across biometrics functions to support efficient and high‑quality clinical development., • Bachelor's degree in Statistics, Mathematics, Life Sciences, Computer Science, or a related discipline; advanced degree preferred., • Extensive leadership and technical experience within Biometrics, including Biostatistics, Statistical Programming., • Demonstrated success managing strategic client relationships within a CRO, pharmaceutical, or biotechnology environment., • Proven experience providing executive oversight across large‑scale clinical development programs and global delivery teams., • Strong understanding of clinical development, regulatory requirements, and biometrics operations., • Ability to influence senior stakeholders and drive alignment across complex, matrixed organizations., • Excellent communication, leadership, and relationship management skills with a track record of building high‑performing teams and delivering business results. 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. • 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 #J-18808-Ljbffr

ICON plc is seeking a Study Start Up Manager for the UK to lead and oversee clinical trial start-up activities, ensuring regulatory compliance and timely activation. You will manage day-to-day site start-up operations and guide a team of start-up professionals to deliver high-quality outcomes. You will collaborate with sponsors, clinical operations, and regulatory groups to meet global requirements, monitor metrics and budgets, and drive process improvements while traveling ~25% as needed. #J-18808-Ljbffr

ICON is seeking a Global Study Manager to be fully integrated in the FSP clinical operations team and deliver global clinical studies. This permanent, home-based role requires managing study activities, vendors, budgets, and regulatory compliance across regions. You will contribute to risk management, quality assurance, and documentation while collaborating with internal teams and external partners. Advanced degree is desirable. #J-18808-Ljbffr

ICON plc is a world-leading healthcare intelligence and clinical research organisation seeking an experienced Pharmacometrics Support Programmer.

We are seeking an experienced Pharmacometrics Support Programmer to join a global FSP team. This is an opportunity for a highly analytical programmer with strong R programming expertise and experience in PK/PD data preparation to contribute to critical drug development programmes.

Join IQVIA on our mission to accelerate innovation for a healthier world!.IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates.Career development opportunities to grow as we grow.AI‑powered career advancement through our internal talent marketp

In 2024, Icon expanded into the UK by bringing Pharmaxo Group into the Icon family, alongside a strategic partnership with Nuffield Health and it’s first cancer centre in Wimbledon, Icon Cancer Centre London. Icon Group was established in 2015 and the businesses that form Icon have been pillars of

ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. In addition to your competit

ICON plc is a world-leading healthcare intelligence and clinical research organization.

You will work hands-on with Java 11, Spring Boot, microservices, AWS, and the ICON IPF Payments framework, collaborating with major banking clients to implement ISO 20022 payment standards and asynchronous.

ICON is committed to providing a workplace free of discrimination and harassment. ICON plc is a world-leading healthcare intelligence and clinical research organization. As a CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, re

ICON plc in Cambridge, UK, is seeking a Clinical Trial Associate to support trial start-up activities and regulatory submissions.

At ICON, inclusion & belonging are fundamental to our culture and values. ICON is committed to providing a workplace free of discrimination and harassment. ICON plc is a world-leading healthcare intelligence and clinical research organization.

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Contract Analyst.

As an Informed Consent Specialist at ICON, you will support the development, review, and management of informed consent documents to ensure they are clear, compliant, and patient-focused. In addition to your competitive salary, ICON offers a range of additional benefits. At ICON, inclusion & belongi

ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. In addition to your competit

ICON plc is a global leader in healthcare intelligence and clinical research.

ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Senior Global Project Manager at ICON, you will be responsible for leading and manage global projects, ensuring successful execution and delivery of project objectives. In addition to your competitive salary

Icon UK Limited is establishing a Cancer Centre in Reading and seeks a qualified Radiation Therapist to deliver high-quality radiotherapy services across treatment, planning, and pre-treatment areas.

ICON plc is seeking a Project Manager to lead General Medicine portfolios, ensuring on-time, on-budget delivery with the highest quality. You will oversee project execution from inception to delivery, coordinate cross-functional teams, and drive continuous improvement while upholding ICON's commitme

ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Contract Analyst at ICON, you will prepare, verify, and carry out invoicing via electronic processing and reporting activities for an assigned portfolio of accounts. In addition to a competitive salary, ICON

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Senior CRA in the UK.

In addition to your competitive salary, ICON offers a range of additional benefits. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values.

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. Are you a current ICON Employee? Please click here to apply. ICO

ICON plc is a world-leading healthcare intelligence and clinical research organization. As an Informed Consent Specialist at ICON, you will support the development, review, and management of informed consent documents to ensure they are clear, compliant, and patient-focused.

Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. ICON is committed to providing a workplace free of discrimination and harassment.

ICON plc is a world-leading healthcare intelligence and clinical research organization.

ICON plc seeks a Senior Clinical Pharmacologist (Director, Clinical Pharmacology) to join a growing client-dedicated team.

At ICON, inclusion & belonging are fundamental to our culture and values. ICON is committed to providing a workplace free of discrimination and harassment. ICON plc is a world-leading healthcare intelligence and clinical research organization.

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