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  • Senior Clinical Scientist  

    ICON
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    Senior Clinical Scientist ICON plc is a world-leading healthcare intel... Read More
    Senior 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 Senior Clinical Scientist to join our diverse and dynamic team. As a Senior Clinical Scientist at ICON, you will play a pivotal role in designing and conducting clinical studies that evaluate the safety and efficacy of innovative treatments. You will contribute to the advancement of groundbreaking therapies through your expertise in clinical trial design, data analysis, and regulatory compliance.What You Will Be Doing:Leading the design and execution of clinical studies, ensuring adherence to protocol and regulatory requirements.Responsible for clinical and scientific execution of protocol(s).Collaborating with cross-functional teams to develop study protocols, informed consent forms, and study reports.Analyzing clinical data and interpreting results to support decision-making and regulatory submissions.Providing scientific input and strategic guidance throughout the clinical development process.Establishing partnerships with key stakeholders to ensure alignment on study objectives and outcomes.Your Profile:Advanced degree in a relevant field such as medicine, life sciences, or pharmacology.Extensive experience in clinical research and study design, preferably within the pharmaceutical or biotechnology industry.Clinical Scientist Experience in pharma or CRO environmentStrong understanding of regulatory guidelines and requirements related to clinical trials.Excellent analytical skills and experience in statistical analysis and data interpretation.Strong communication, interpersonal, and leadership skills, with the ability to influence and drive results in a collaborative environment.#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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  • Central Monitor  

    ICON
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    Central Monitor ICON plc is a world-leading healthcare intelligence an... Read More
    Central Monitor 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. Job title - Central MonitorLocation - Bulgaria, Poland, UK, Belgium  (remote) Fully sponsor dedicatedWorking fully embedded within a growing program at ICON, you will play a key role in overseeing and supporting clinical trials through centralized monitoring activities. This role ensures data quality, identifies potential risks, and enhances trial oversight by leveraging data analytics and risk-based monitoring strategies.Role Accountabilities Central Monitoring Execution:Implement and execute centralized monitoring strategies to support clinical trial oversight.Conduct ongoing central monitoring analysis of clinical trial data to detect trends and signals.Work with Data Analysts team in reviewing Central Monitoring technology outputs and performing an initial investigation of identified risks (e.g., atypical data patterns) to assess their scope and nature in preparation for review with study teams.Interpret the study protocol to define key data for analysis; support Data Analysts in defining key data.Ensure adherence to risk-based monitoring plans, SOPs, and industry best practices.Risk Identification and Management:Perform risk assessments based on data review, identifying potential site or trial risks.Collaborate with Lead Central Monitor and study teams to refine and implement risk-based monitoring plans.Provide insights and recommendations to enhance trial efficiency and mitigate risks.Support root cause analysis for identified issues and suggest corrective actions.Data Review and Reporting:Generate and summarize findings (Central Monitoring reports and dashboards) and lead the communication of results to study teams (both written report and oral presentation). Contribute to GCO understanding of impact of findings to data quality.Support DQT in assessing the criticality and potential root causes of the findings and in defining appropriate follow-up actions.Support study teams in adopting an approach to clinical trial monitoring that utilizes data and site level information to determine needs for performing on-site, remote and centralized monitoring activities and focuses resources on risks that have the most potential to impact patients’ safety and data quality.Document findings, escalate critical risks, and support follow-up actions.Ensure timely documentation of monitoring activities and findings.Collaboration and Cross-Functional Engagement:Collaborate with cross-functional study teams, including Risk Surveillance Leads, Study Leaders, Data Managers, and Clinical Scientific Leaders, to ensure robust risk mitigation plans are in place and effectively executed.Participate in study team meetings and provide data-driven recommendations.Act as a single point of contact for Central Monitoring activities for relevant stakeholders for allocated studies and ensure timely communication and coordination.Act as a key interface between Central Monitoring, Clinical Study Teams, and Investigators.Protocol and Study Design Support:Advise on the design and optimization of KRIs and thresholds to enhance the efficacy of Central Monitoring efforts.Continuous Improvement and Compliance:Support the continuous improvement of centralized monitoring methodologies.Ensure adherence to regulatory requirements, SOPs, and Good Clinical Practice (GCP) guidelines.Contribute to training and knowledge-sharing initiatives within the Central Monitoring team. Client role requirements:≥ 5 years of recent pharmaceutical industry experience, with previous experience in clinical research, in a Pharmaceutical Industry or CROs. Strong clinical experience with excellent understanding of clinical trial development and risk management processes and the management of clinical trials. Specific central monitoring / monitoring experience are strongly preferred.≥ 3 years comprehensive experience in monitoring (central), clinical data analytics, data management activities or equivalent.Knowledge of overall clinical trial management process, understanding of the protocol, study associated risks and their significance, and the risk management process.Thorough understanding of the international aspects of drug development process, including expert knowledge of international standards (GCP/ICH), health authorities, and our clients standards.Critical thinking and analytical skills to understand/analyze complex data and provide insight into risk signaling, trends, and outliers in data.Excellent communication and coordination skills.Strong capability in working in a Global/Country matrixed environment. Organizational awareness, including significant experience working cross- functionally.Strong technical, analytical and quantitative problem-solving skills. Technical ability to use the relevant technology and risk-based tools/platforms effectively.Data and Digital expertise: experience working with e-databases, clinical and/or project management planning and reporting and analytics systems.Strong project management skill with demonstrated ability to meet timelines.Understanding team dynamics: recognizing the diverse talents, personalities, and working styles within a team to create a connected and productive work environment.Experience in transformation, leveraging AI and analyticsAbility to understand and navigate diverse cultural contexts. This includes fostering inclusive environments and developing talents across different countries.Extensive knowledge of appropriate therapeutic area preferred 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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  • Clinical Scientist  

    ICON
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    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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  • Randomization & Trial Supply Manager - Demand Planning  

    ICON
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    Demand Planning System Manager - RTSM ICON plc is a world-leading heal... Read More
    Demand Planning System Manager - RTSM 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 Randomization & Trial Supply Manager (RTSM) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Delivering Excellence and Quality for Studies in a Diverse PortfolioAccountable for the User Acceptance Testing (UAT) process for IRT systems. Through UAT, you will be key to the clinical trial process by are ensuring quality and proper functionality in a highly critical system. While following an established process, you’ll also be expected to make suggestions and deploy new ways of working that create efficiencies while maintaining effectiveness.  We are therefore seeking candidates with a unique mix of experience and openness to improvements.The job tasks will include:While working with the study-responsible RTSM Manager, develop an understanding of IRT requirements for the trialApply that understanding of the requirements and trial to create a Testing Plan and Tests that will rigorously stress the IRT system built by the IRT suppliersDemonstrate sufficient knowledge of randomization and medication assignment processes to be able to perform required un-blinded assessments of the IVR/IWR system performance (or functionality) should that be assigneIdentify and resolve issues identified during the testing processCreate and store documentation of these tasksTrack trends identified in UAT with the goal of identifying problematic areas that can be proactively addressed to prevent recurrenceYour Profile:At least 6 years operational experience in clinical trials with a pharmaceutical company and/or a Clinical Research Organization is requiredStrong knowledge of the clinical trial process, especially with randomization and trial supply management (RTSM) activities and systemsExperience with testing or validation activities in the clinical trial environmentExperience with IVRS/IWRS suppliers is preferredEnd to End experience for IRT system buildsProject Management experience a plus.Accountable for system development.Vendor mangament experience. Ability to identify issues and problem solve independently while in a complex environmentBA/BS degree required. #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
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  • CRA  

    ICON
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    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
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  • Clinical Data Engineer  

    ICON
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    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
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  • Senior Director, Biostatistics Consulting  

    ICON
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    Senior Director, Biostatistical Consulting ICON plc is a world-leading... Read More
    Senior Director, Biostatistical Consulting 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 Director, Biostatistics Consulting to join our diverse and dynamic team. As a Senior Director, you will play a pivotal role in leading our biostatistics consulting practice by providing expert guidance on optimal statistical design,  helping with regulatory agency negotiations, and guiding the strategic direction of clinical research programs in collaboration with therapeutic area experts.  You will contribute to the success of our clients through your expertise in statistical design and interpretation of results, perspective on successful strategies across different therapeutic areas and by providing insight on likely regulatory agency acceptance of your proposed options.What You Will Be Doing:Leading the biostatistics consulting practice, overseeing the development and implementation of statistical strategies and methodologies to support clinical research and regulatory approval.Providing expert biostatistical guidance on study design, statistical analysis, and data interpretation to ensure high-quality and scientifically valid results.Collaborating with cross-functional teams, including clinical and regulatory affairs, to align biostatistical approaches with study objectives and regulatory requirements.Developing and implementing best practices for statistical consulting, ensuring adherence to industry standards and promoting innovative solutions for complex statistical challenges.Building and maintaining strong relationships with clients and stakeholders, delivering expert consulting services, and driving strategic growth in the biostatistics practice.When required attending sponsor meetings with regulatory authorities.Your Profile:Advanced degree in biostatistics, statistics, or a related field, with significant experience in biostatistics consulting and clinical trial support.Extensive experience in designing and analysing clinical trials, with a deep understanding of regulatory requirements and statistical methodologies.Working knowledge of the application of Bayesian methodologies in a clinical research environment.Proven track record of leading and managing biostatistics teams, with strong expertise in strategic planning and client management .Excellent problem-solving skills, with the ability to address complex statistical issues and drive innovative solutions.Proven track record of authoring the statistical sections of regulatory submissions and responding to regulatory questions .Outstanding communication, interpersonal, and leadership skills, with the ability to present complex statistical concepts clearly and collaborate effectively with stakeholders across the organization.#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
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  • Sr Dir, Nonclin/Preclin Drug Dev Services  

    ICON
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    Senior Director, Nonclinical/Preclinical Drug Development Services ICO... Read More
    Senior Director, Nonclinical/Preclinical Drug Development Services 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 Director, Nonclinical/Preclinical Drug Development Services to join our diverse and dynamic team. As a Senior Director in this role at ICON, you will be responsible for overseeing and guiding nonclinical and preclinical drug development services, ensuring that our clients receive high-quality support throughout the drug development lifecycle. You will contribute to advancing innovative therapies by providing strategic leadership, fostering collaborations, and driving operational excellence in nonclinical study design and execution.What You Will Be Doing:
    Leading the development and execution of nonclinical and preclinical drug development strategies to support client projects.Managing cross-functional teams to ensure successful study design, implementation, and regulatory compliance.Building and maintaining strong relationships with clients, stakeholders, and regulatory agencies to facilitate project success.Identifying opportunities for process improvements and innovation within nonclinical and preclinical services.Providing mentorship and guidance to team members, fostering a culture of collaboration and continuous improvement.Your Profile:
    Advanced degree (Ph.D. or equivalent) in a relevant scientific field, such as pharmacology, toxicology, or biomedical sciences.Extensive experience in nonclinical or preclinical drug development, with a proven track record of leadership in the pharmaceutical or biotechnology industry.Strong understanding of regulatory requirements and guidelines related to nonclinical studies.Exceptional leadership and project management skills, with the ability to drive results in a fast-paced environment.Excellent communication and interpersonal skills, with the ability to influence stakeholders and build effective partnerships. 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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  • Senior Director DMPK - Nonclinical Consulting  

    ICON
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    Senior Director DMPK - Nonclinical Consulting ICON plc is a world-lead... Read More
    Senior Director DMPK - Nonclinical Consulting 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 Director, with extensive expertise in Drug Metabolism and Pharmacokinetics (DMPK), to join our nonclinical consultancy team. As a Senior Director at ICON, you will work closely with other team members to provide expert scientific and strategic advice to our customers. This role is fully remote.
    What you will be doing Providing expert knowledge of DMPK requirements on a variety of different projects, including small molecules and biopharmaceuticals, such as ADCs.Conducting in-depth review of nonclinical programmes to identify any gaps in the data package ahead of regulatory submission.Troubleshooting specific issues related to DMPK and strategising solutionsPreparing written sections of regulatory submission documents pertaining to DMPK, including IBs and eCTD Modules.Identification of appropriate nonclinical CROs and placement / monitoring of DMPK studies on behalf of ICON’s customers.Engaging and driving business development initiatives.Your profile Batchelor of Science (BSc) or above with minimum of 20 years experience in pharmaceutical development, including at least 10 years’ experience working as a DMPK subject matter expert (SME), with in depth knowledge of in vitro and in vivo assays, bioanalytical techniques and pharmacokinetic interpretation / modelling.Proven track record of decision making, planning and organising.A sound understanding of current regulatory guidelines and expectations for nonclinical ADME requirements across all phases of clinical development.Excellent communication and interpersonal skills, with the ability to represent the nonclinical team effectively both internally and externally.Self-motivated and confident to work independently with minimal supervision, but also an excellent team player.  Ideally experience and a desire to take on a leadership role within the group.Some domestic and international travel is required from time to time, so a valid Driver's license and Passport is required.#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
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