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ICON
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  • Senior Director, Biostatistics Consulting  

    - Reading
    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, providing expert statistical guidance, and driving the strategic direction for biostatistical support in clinical trials. You will contribute to the success of our projects by delivering high-quality statistical analysis, ensuring regulatory compliance, and enhancing data-driven decision-making across our organization.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 submissions.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
  • Senior CRA  

    - Reading
    SCRA ICON plc is a world-leading healthcare intelligence and clinical... Read More
    SCRA 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 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
  • 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
  • Learning & Development Specialist  

    - Swansea
    Learning & Development Specialist ICON plc is a world-leading healthca... Read More
    Learning & Development Specialist 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 Learning & Development Specialist to join our diverse and dynamic team. As a Learning & Development Specialist at ICON, you will play a critical role in designing, delivering, and evaluating training programs that enhance the skills and capabilities of our workforce. You will contribute to building a culture of continuous learning by developing innovative learning solutions that meet the evolving needs of the organization.What You Will Be Doing:Designing and delivering engaging learning and development programs for employees at all levels.Collaborating with department leaders to identify skill gaps and create tailored training solutions.Evaluating the effectiveness of training initiatives and implementing improvements as necessary.Facilitating in-person and virtual training sessions to ensure a high-quality learning experience.Managing and updating the learning management system (LMS) to track and report on training activities.Your Profile:Bachelor’s degree in Human Resources, Education, or a related field.Experience in designing, developing, and delivering learning programs in a corporate environment.Strong facilitation and presentation skills, with the ability to engage diverse audiences.Excellent project management and organizational skills.Proficiency with learning management systems (LMS) and e-learning tools. 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 Associate I  

    - Warwick
    Patient Recruitment Associate I ICON plc is a world-leading healthcare... Read More
    Patient Recruitment Associate I 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 Associate to join our diverse and dynamic team. As a Patient Recruitment Associate at ICON, you will be instrumental in developing and executing strategies to identify, engage, and enroll patients in clinical trials, ensuring that studies are adequately powered to meet their objectives. Your strong interpersonal skills and understanding of the patient experience will be essential in fostering relationships and enhancing patient recruitment efforts.What You Will Be Doing:Collaborating with clinical teams to design and implement effective patient recruitment strategies tailored to specific clinical trials.Engaging with patients, healthcare providers, and community organizations to raise awareness of clinical trial opportunities.Monitoring recruitment progress and identifying barriers to enrollment, implementing solutions to enhance patient participation.Collecting and analyzing recruitment data to evaluate the effectiveness of strategies and inform ongoing improvements.Ensuring compliance with regulatory requirements and best practices in patient recruitment and engagement.Your Profile:Bachelor's degree in life sciences, healthcare, social sciences, or a related field.Experience in patient recruitment, clinical research, or healthcare, with a strong understanding of the patient journey.Excellent communication and interpersonal skills, with the ability to build rapport with diverse patient populations.Strong organizational skills and attention to detail, with the ability to manage multiple projects effectively.A commitment to enhancing the patient experience and promoting the importance of clinical trial participation.Temporary position (6months)Hybrid Warwickshire#LI-LR1 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
  • IP Administration - Nurse  

    IP Administrator - Nurse ICON plc is a world-leading healthcare intell... Read More
    IP Administrator - Nurse 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 Site Investigational Product Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:You will be dedicated to one of our global pharmaceutical clients, a company that values performance, recognises merit and has a high focus on quality. This environment encourages innovation, individuality and embraces people that want to be a part of it.The Site Investigational Product Specialist will serve as a key contact point between the sponsor and the investigational site for Investigational Product Preparation Instructions (IPPI) training of studies with a complex IP preparation process. This role will focus on IPPI review and training/implementation of IP preparation steps for all compounds deemed requiring training plans. The Site Investigational Product Specialist will be the key internal and external interface to ensure overall IPPI adherence . He/she will contribute to continuous process improvement, training and mentoring for IPPI.The tasks undertaken are varied and can include:Play a key role in the safe, efficient and effective Investigational Product preparation and administration in clinical trials.Review and provide input on Investigational Product Preparation Instructions Site Investigational Product Procedures Manual, monitoring guidelines and all specific forms related to Investigational Product preparation and dosing before finalization as applicable.Process risk assessment review where applicable.Close collaboration with the Drug Product Development team and the Drug Preparation Administration Team.Early connection with investigational site pharmacy and nursing staff to review site IP process and equipment.Close collaboration with (Global Trial Lead) GTL, (Study Manager) SM, (Trial Manager) TM, Independent Drug Monitor (IDM) and Pharmacy Investigational Product Specialist (PIPS) for all IPPI related topics.Evaluate and support process for IP ancillary supplies/administration kits are compatible with the site equipment/practice in the country/investigational site.Review of site's dispensing and accountability records to ensure key information is captured to confirm dose delivery and administration is documented e.g. infusion rates/volumes.Collaboration on Investigational Product training material development with key stakeholders.Observe first dosing on site and/or support SM/IDM/PIPS if allowed according to local guidelines and blinding requirements.Point of contact for the internal study team in the country for questions related to the IP administration.Review any modification of IPPI, SIPPM manual, specific forms related to IP administration and dosing during the applicable phases of the trial.Establish and maintain good and productive working relationships with internal and external stakeholders (e.g. nurses, investigators,…).You are:A degree in general nursing is required.3- 4 years of recent clinical/hospital experience is required;Experience in antibody treatment, (Oncology (hematology and solid tumor) and / or Immunology Therapeutic Area)Min. 3 years’ experience with various IP administration routes (IV, SC, IM)Clinical trial research experience.Minimum of 5+ years of recent clinical/hospital experience is required; however, other relevant experience may be considered by the hiring manager when considering the candidate’s eligibility.Minimum of 5+ years’ experience with various IP administration routes (IV, SC, IM, intravesical, intraperitoneal, blood- and cell products) and priming and flushing procedures required.Extensive knowledge on Administration related requirements (background of anatomy and physiology, metabolism of drugs and IP, hygienic requirements, how to handle hazardous drugs)#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
  • HR Manager - 12 month FTC  

    - Reading
    HR Manager -12 month FTC - UK - 3 days in Reading office and 2 days fr... Read More
    HR Manager -12 month FTC - UK - 3 days in Reading office and 2 days from home 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 an HR Manager to join our diverse and dynamic team. As an HR Manager at ICON, you will play a key role in overseeing HR operations and providing strategic guidance on people-related initiatives. Your guidance and leadership will be essential in promoting a positive, inclusive work culture and aligning HR practices with organizational goals.This role is based at our welcoming and contemporary offices in Reading (Green Park). Hybrid - 60% office based.What You Will Be Doing:Managing and supporting HR activities, with a strong focus on employee relations, performance management, and talent development.Partnering with senior management to develop and implement HR strategies that support business objectives and foster a high-performing culture.Ensuring compliance with HR policies, employment laws, and industry regulations across the organization.Analyzing HR metrics and trends to drive strategic decision-making and identify areas for improvement.Your Profile:Bachelor's degree in human resources, business administration, or a related field, or equivalent experience.Extensive experience in generalist HR management, preferably within a large or global organization.Strong understanding of HR best practices, in particular employee relations, and talent management.Excellent leadership and interpersonal skills, with the ability to influence and engage stakeholders at all levels.A commitment to fostering an inclusive, collaborative work environment that supports employee growth and well-being. 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 Trial Manager, Haematology  

    - Reading
    Clinical Trial Manager, Haematology (UK) ICON plc is a world-leading h... Read More
    Clinical Trial Manager, Haematology (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. ICON Plc is a global leader in clinical research, driven by innovation, collaboration, and a shared mission to improve patient outcomes. We are currently seeking a home or office-based Haematology Clinical Trial Manager to partner with one of our Global Pharmaceutical partners.The RoleIn this critical role, you will be responsible for the planning, execution, and successful completion of haematology clinical trials, ensuring delivery to agreed timelines, budgets, and regulatory standards. As a key leader within our research organization, you will provide strategic oversight, foster strong cross-functional collaboration, and ensure operational excellence throughout the trial lifecycle.Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.Collaborate with cross-functional teams (with some overseeing responsibilities) to establish and implement clinical trial protocols and procedures.Build and manage strong relationships with trial investigators and stakeholders.Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.Your ProfileUniversity degree in medicine, science, or equivalent combination of education & experienceDemonstrated ability to drive the clinical deliverables of a studySubject matter expertise in the designated therapeutic areaPrior monitoring experience as a CRA and Trial Manager experience in a commercial capacity.Those with Haematology experience are 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
  • Global Data Manager  

    Global Data Manager ICON plc is a world-leading healthcare intelligenc... Read More
    Global Data 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. Global Data Manager, Sponsor DedicatedUK or South AfricaWe are currently seeking a Senior Clinical Data Science Lead to join our diverse and dynamic team. As a Senior Clinical Data Science Lead at ICON, you will play a pivotal role in leading the analysis, interpretation, and management of clinical data to drive the success of our clinical trials. You will contribute to the advancement of innovative treatments and therapies by overseeing data science initiatives and ensuring data quality and integrity across studies.What You Will Be Doing:Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting.Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs.Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes.Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements.Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research.Your Profile:Advanced degree in a relevant field such as data science, biostatistics, or life sciences.Extensive experience in clinical data science, with a strong focus on data management and analysis in clinical trials.Strong leadership skills and a proven ability to manage cross-functional teams in a fast-paced, matrix environment.Expertise in data analysis tools, statistical software, and data visualization techniques.Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive change in a complex organization.#LI-JC3#LI-Remote 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
  • CRA UK - Oncology experience required  

    CRA - Oncology focused ICON plc is a world-leading healthcare intellig... Read More
    CRA - Oncology focused 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 - Clinical Research Associate (2+ years' Oncology experienced required) Location - Must be based in the UK 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 (3+ years), 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 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

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