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  • Senior CRA  

    Sr CRA ICON plc is a world-leading healthcare intelligence and clinica... Read More
    Sr CRA 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. Role: Senior CRA (Must have 7 years' experience minimum working as a CRA) Location: Must be based in the UK - nationwide travel Fully sponsor dedicatedWe are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.Your Profile:Advanced degree in a relevant field such as life sciences, nursing, or medicine.Extensive experience as a Clinical Research Associate, (7+ years' minimum required) with a strong understanding of clinical trial processes and regulatory requirements.Must have at least 2 years' experience working on Oncology studiesProven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Senior Clinical Research Associate  

    Senior Clinical Research Associate - UK ICON plc is a world-leading he... Read More
    Senior Clinical Research Associate - UK 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 Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.Your Profile:Advanced degree in a relevant field such as life sciences, nursing, or medicine.Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s licenseRequired SkillsPhase I Oncology Expertise: Strong background in early-phase oncology trials, including safety, PK/PD, and dose-escalation studies.Indication-Specific Knowledge: Experience with breast, ovarian, prostate, and pancreatic cancer clinical trials.Investigational Product Familiarity: Prior exposure to PARP inhibitors (a plus but not mandatory).Traditional Monitoring Model: Solid skills and proficiency in on-site monitoring, full source data verification, IP accountability and regulatory compliance.Trip Report Writing: Proven ability to produce detailed, accurate, and timely monitoring visit reports. Extensive experience working with a CTMS platform (Siebel CTMS, Veeva Vault CTMS, Medidata CTMS, Oracle Clinical/Clinical One, or others). 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Clinical Data Configuration Engineer FSP - SDTM Programming/mapping  

    - Livingston
    Clinical Data Configuration Engineer FSP - SDTM Programming/mapping IC... Read More
    Clinical Data Configuration Engineer FSP - SDTM Programming/mapping 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 Clinical Data Configuration Engineer FSP - SDTM Programming/mapping to join our diverse and dynamic team. In this role, you will play a pivotal role in designing and implementing advanced clinical systems that enhance trial design and execution. Your expertise will be essential in driving innovation and ensuring that our clinical systems meet regulatory requirements and support operational efficiency.
    What You Will Be Doing:
    • Leading the design and development of clinical systems, ensuring alignment with study protocols and operational needs.
    • Collaborating with cross-functional teams to identify opportunities for system enhancements and innovations in clinical trial processes.
    • Overseeing system configuration, integration, and testing to ensure optimal functionality and user experience.
    • Providing strategic guidance on the implementation of new technologies and best practices in clinical system design.
    • Staying current with industry trends and advancements in clinical technology to drive continuous improvement initiatives.Your Profile:• Master degree in Computer science or relevant field• 5 years work experience in similar role• Strong SDTM and CDISC standards knowledge.• Experience in SDTM specification creation, review, and ownership (not just execution).• Ability to make mapping decisions based on standards and processes.• Experience in SDTM mapping rules, variable derivations, and study-specific/global standards interpretation.• QC experience to ensure team adherence to standards.• Contribution to SDTM or standards development as needed.• Familiarity with SAS and R for implementing specifications (programming is secondary).• Understanding of end-to-end data flow from raw data to completed SDTM datasets.• Ideal candidates may have worked in data standards teams with an SDTM focus. 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Clinical Data Engineer  

    - Reading
    Clinical Data Engineer ICON plc is a world-leading healthcare intellig... Read More
    Clinical Data Engineer 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 Clinical Data Engineer, you’ll step into a fully remote, high-visibility role within the world’s largest and most comprehensive clinical research organization—powered by healthcare intelligence and driven by innovation. In this client-dedicated position, you’ll work hand-in-hand with a top global pharmaceutical client, becoming a key technical partner shaping the future of their clinical data platform. You’ll lead the design and delivery of next-generation, enterprise-scale data pipelines, and analytics technologies to transform how clinical trial data is ingested, integrated, and analyzed. From building cutting-edge ingestion frameworks to enabling regulatory-ready, real-time insights, your work will sit at the intersection of modern technology and life-changing science—driving faster decisions, smarter trials, and better patient outcomes, all from a 100% remote setting.What you will be doing:Serve as a technical expert in building data pipelines for the ingestion and delivery of clinical data at the study level, supporting study start-up, conduct, and close-out activities.Develop robust data pipelines for integrating heterogeneous data sources.Identify, design, and implement scalable data delivery solutions, automating manual processes whenever possible.Develop and implement comprehensive data integrity and quality checks throughout the data ingestion process.Design and build infrastructure for optimal data extraction, transformation, and loading (ETL/ELT) using cloud platforms such as AWS and Azure.Collaborate with downstream users—including statistical programmers, SDTM programmers, analytics, and clinical data programmers—to ensure deliverables meet end-user requirements.Appropriately escalate issues to CDE leadership as needed.You are:Bachelor’s degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field; advanced degree preferred.8+ years of experience in data engineering or a related field, with at least 5 years focused on building pipelines for complex, multi-source data integration. Extensive experience developing ELT and ETL solutions for data warehouses and data lakes.Proficient with Python, R, RShiny, SQL, and NoSQL databases.Hands-on cloud experience with AWS, Azure, or GCP.Familiarity with GitLab, GitHub, and Jenkins for version control and CI/CD.Proven expertise in deploying data pipelines in cloud environments.Skilled in setting up and managing data warehouses and data lakes (e.g., Snowflake, Amazon Redshift).Efficient in designing, developing, and maintaining scalable data pipelines for large datasets.Strong understanding of database concepts, with working knowledge of XML, JSON, and API integrations. 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Regulatory Scientist  

    - Reading
    Regulatory Scientist ICON plc is a world-leading healthcare intelligen... Read More
    Regulatory Scientist 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 Regulatory Scientist to join our diverse and dynamic team. As a Regulatory Scientist at ICON, you will support the development, implementation, and execution of regulatory strategies for clinical development programmes. You will contribute scientific and regulatory expertise to ensure submissions meet global requirements and support successful product development.What You Will Be Doing:Contributing to regulatory strategy development for clinical programmes, including plans for health authority interactions and submissions.Preparing, reviewing, and coordinating regulatory documents such as clinical trial applications, briefing packages, and responses to health authority questions.Interpreting and applying relevant regulations, guidelines, and precedents to support compliant study design and execution.Collaborating with clinical, safety, CMC, and other cross-functional teams to ensure alignment of regulatory content and messaging.Monitoring changes in the regulatory environment and providing guidance on potential impact to programmes and submissions.Supporting regulatory interactions and meetings, including preparation of materials and documentation of outcomes.Your Profile:Advanced degree in life sciences, pharmacy, or a related field, or equivalent scientific and regulatory experience.Experience in regulatory affairs, with experience of UK submissions, regulatory writing, or clinical development within the pharma, biotech, or CRO industry.Good understanding of global regulatory frameworks and guidelines relevant to clinical development.Strong scientific, analytical, and critical thinking skills, with the ability to interpret complex data and regulations.Excellent written and verbal communication skills, with high attention to detail and accuracy.Ability to work effectively in cross-functional teams and manage multiple regulatory activities and timelines.#LI-CL1 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Clinical Research Physician  

    - Crayfield
    Clinical Research Physician - South London ICON plc is a world-leading... Read More
    Clinical Research Physician - South London 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. Clinical Research Physician Clinic based - Orpington, South London 4 days a week.We are currently seeking a Clinical Research Physician to join our diverse and dynamic team. As a Clinical Research Physician at ICON, you will play a vital role in leading clinical trials, ensuring that they are conducted ethically and in compliance with regulatory standards. You will contribute to the advancement of innovative therapies by providing medical expertise and overseeing the safety and efficacy of clinical studies.What You Will Be Doing:Leading the design and execution of clinical trial protocols, ensuring alignment with scientific and regulatory guidelines.Monitoring patient safety and overseeing the clinical aspects of trials to ensure compliance with GCP standards.Collaborating with cross-functional teams to analyze study data and provide medical insights that guide decision-making.Engaging with investigators and study sites to ensure adherence to protocols and facilitate successful trial execution.Contributing to the preparation of regulatory submissions and clinical study reports.Your Profile:Medical degree (MD or equivalent) with relevant clinical research experience.Strong understanding of clinical trial processes and regulatory requirements.Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.Effective communication and interpersonal skills, with the ability to engage with diverse stakeholders.Demonstrated ability to work collaboratively in a fast-paced, team-oriented environment.#LI-CL1 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Patient Recruitment Manager  

    Patient Recruitment Manager ICON plc is a world-leading healthcare int... Read More
    Patient Recruitment Manager 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 Patient Recruitment Manager to join our diverse and dynamic team. As a Patient Recruitment Manager, you will be responsible for strategizing and overseeing patient recruitment initiatives for clinical trials. You will work collaboratively with cross-functional teams to ensure that recruitment efforts are effective, efficient, and aligned with the goals of the studies, ultimately enhancing patient access and engagement.What You Will Be Doing:Developing and executing comprehensive patient recruitment strategies tailored to specific clinical trial objectives, ensuring alignment with study protocols and timelines.Leading cross-functional teams in the identification and engagement of target patient populations, utilizing data-driven insights to optimize recruitment efforts.Building and maintaining partnerships with healthcare providers, patient advocacy groups, and community organizations to enhance recruitment and retention strategies.Analyzing recruitment metrics and performance data to identify trends, challenges, and opportunities, making data-informed recommendations for improvement.Creating and overseeing the development of patient-centric marketing materials and outreach campaigns to effectively communicate trial benefits and address patient concerns.Providing training and guidance to project teams and staff on recruitment best practices, tools, and techniques to enhance recruitment success.Staying informed about industry trends, regulatory guidelines, and emerging technologies that impact patient recruitment and engagement.Monitoring recruitment progress and outcomes, reporting on successes and challenges to senior leadership and stakeholders.Your Profile:Bachelor’s degree in life sciences, healthcare, marketing, or a related field. An advanced degree is preferred.Extensive experience in patient recruitment or clinical research, with a proven track record of successful recruitment strategies in a clinical trial setting.A minimum of 7 years of progressive business experience, demonstrated and proven performance in strategic and/or digital marketing and/or clinical operations experience (clinical operations experience would be preferably specific to patient recruitment/retention & site engagement) is requiredExperience in the following critical competencies is required: Strategy Development & execution, Analysis, Customer & Market Landscape Knowledge, Medical StrategyStrong leadership skills, with the ability to motivate and guide cross-functional teams toward achieving recruitment goals.Excellent communication and interpersonal skills, with the ability to build relationships with diverse stakeholders and effectively advocate for patient participation.Strong analytical skills, with experience in evaluating recruitment performance metrics and using data to drive strategic decisions.Creative problem-solver with a passion for improving patient access to clinical trials and enhancing the overall patient experience.Proficiency in digital marketing strategies and tools, as well as familiarity with social media platforms for outreach efforts.Experience of successfully working a heavily matrix organization. Willingness to travel for outreach initiatives, conferences, and stakeholder meetings as needed.#LI-Remote#LI-RS1 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Senior CRA / CRA II  

    - Reading
    Senior CRA / CRA II ICON plc is a world-leading healthcare intelligen... Read More
    Senior CRA / CRA II 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 Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA for the Full-Service team at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.Your Profile:Advanced degree in a relevant field such as life sciences, nursing, or medicine.Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.Ability to travel (domestic fly/drive) across the UK (approx. 6-8 days per month).Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Study Delivery Lead in Non-Interventional studies  

    Global Study Delivery Lead/Non-Interventional/ Home-based ICON plc is... Read More
    Global Study Delivery Lead/Non-Interventional/ Home-based 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 Global Clinical Project Manager to join our diverse and dynamic team. As a Project Manager at ICON, you will be responsible for leading and coordinating project activities in Non-Interventional studies, ensuring that projects are delivered on time, within budget, and to the highest quality standards. Your role will involve overseeing all aspects of project execution, from planning and resource management to stakeholder communication and risk mitigation.What You Will Be Doing:Developing and managing detailed project plans, including timelines, budgets, and resource allocation to ensure successful project delivery.Leading cross-functional project teams, coordinating efforts to meet project objectives, and facilitating effective communication and collaboration.Monitoring project progress, identifying potential risks and issues, and implementing strategies to address challenges and keep projects on track.Engaging with stakeholders to manage expectations, provide updates, and ensure alignment with project goals and organizational objectives.Preparing and presenting project reports, status updates, and performance metrics to senior management and other stakeholders.Your Profile:Bachelor’s degree in project management, business, or a related field is preferred, with significant experience in project management and team leadership.Proven track record of successfully managing projects from inception to completion, with a focus on delivering results within scope, time, and budget constraints.Strong leadership and organizational skills, with the ability to effectively manage project teams and prioritize tasks.Excellent communication and interpersonal skills, with the ability to build relationships and manage stakeholder expectations.Proficiency in project management tools and methodologies, with certifications such as PMP or PRINCE2 being advantageous.Detail-oriented, proactive, and adaptable, with a commitment to achieving project goals and driving continuous improvement. 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. Are you a current ICON Employee? Please click here to apply Read Less
  • Clinical Scientist  

    Clinical Scientist ICON plc is a world-leading healthcare intelligence... Read More
    Clinical Scientist 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 Clinical Scientist to join our diverse and dynamic team. As a Clinical Scientist at ICON, you will play a critical role in designing and conducting clinical studies that advance our understanding of new therapies. You will contribute to the development of innovative treatments by applying scientific expertise and collaborating with multidisciplinary teams throughout the research process.What You Will Be Doing:Designing and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards.Conducting data analysis and interpretation to derive insights that support study objectives.Collaborating with cross-functional teams to ensure effective study execution and data quality.Engaging with stakeholders to communicate findings and contribute to scientific discussions.Assisting in the preparation of regulatory submissions, study reports, and scientific publications.Your Profile:Advanced degree in life sciences, medicine, or a related field.Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes.Excellent analytical skills and proficiency in data interpretation and statistical analysis.Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams.Detail-oriented and committed to maintaining high standards of data integrity and quality.#LI-Remote#LI-NR1 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. Are you a current ICON Employee? Please click here to apply Read Less

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany