18 Clinical Informatics jobs in the United Kingdom

Our client, a prestigious global Legal firm, is seeking a highly skilled and detail-oriented Senior Clinical Data Manager to join their team. This is a fully remote position, offering the flexibility to work from anywhere within the UK.

In this vital role, you will be responsible for the end-to-end management of clinical trial data, ensuring its accuracy, integrity, and compliance with regulatory standards. You will lead data management activities for multiple clinical studies, collaborating closely with clinical operations, biostatistics, and regulatory affairs teams.

Key responsibilities include developing and implementing data management plans, designing clinical databases, managing data validation processes, and overseeing data cleaning activities. You will ensure that all data management activities adhere to Good Clinical Practice (GCP) guidelines and relevant data privacy regulations. Experience with various Electronic Data Capture (EDC) systems and a strong understanding of clinical trial processes are essential.

The ideal candidate will possess a Bachelor's or Master's degree in a relevant scientific or healthcare field, with extensive experience in clinical data management. Strong leadership and project management skills are required, along with excellent analytical and problem-solving abilities. You must be adept at interpreting complex data, identifying potential issues, and implementing effective solutions. Exceptional communication and interpersonal skills are crucial for collaborating with internal teams and external partners. This is an exceptional opportunity for an experienced data professional to make a significant contribution to life-changing research.

Responsibilities:

• Lead and manage all aspects of clinical data management for assigned studies.
• Develop and implement comprehensive Data Management Plans (DMPs).
• Design, build, and maintain clinical databases using EDC systems.
• Define data validation rules and perform data cleaning activities to ensure data integrity.
• Oversee user acceptance testing (UAT) of clinical databases.
• Generate data management reports and metrics for study progress.
• Ensure compliance with GCP, ICH guidelines, and data privacy regulations (e.g., GDPR).
• Collaborate with Clinical Operations, Biostatistics, and Medical teams to address data-related queries.
• Participate in the selection and implementation of new data management technologies.
• Contribute to the development and training of junior data management personnel.

Qualifications:

• Bachelor's or Master's degree in Life Sciences, Computer Science, Statistics, or a related field.
• Minimum of 7 years of progressive experience in clinical data management.
• Proven experience managing data for Phase I-IV clinical trials.
• Proficiency with multiple Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC).
• Strong understanding of clinical trial processes and regulatory requirements (GCP, ICH).
• Excellent understanding of database design, data validation, and data reconciliation.
• Strong analytical, problem-solving, and critical thinking skills.
• Exceptional written and verbal communication skills.
• Ability to manage multiple projects simultaneously and prioritize tasks effectively.
• Experience with data standardization (e.g., CDISC SDTM/ADaM) is highly desirable.

This fully remote role offers a chance to be at the forefront of clinical research data integrity.

Our client, a globally recognized pharmaceutical company at the forefront of innovative drug development, is actively seeking a highly skilled and experienced Senior Clinical Data Manager to join their expanding, fully remote team. In this critical role, you will be instrumental in ensuring the integrity, quality, and timeliness of clinical trial data across multiple therapeutic areas. You will be responsible for the design, development, and implementation of data management plans (DMPs), database setup, data validation strategies, and end-user training. Your expertise will be vital in overseeing the end-to-end data management process, from database lock to archiving, ensuring compliance with all relevant regulatory guidelines (e.g., ICH GCP, FDA). This position demands a meticulous approach to data handling, meticulous attention to detail, and a deep understanding of clinical trial methodologies and data standards (CDISC SDTM/ADAM). You will collaborate closely with internal stakeholders, including Clinical Operations, Biostatistics, and Statistical Programming, as well as external partners such as Contract Research Organizations (CROs). Responsibilities include leading data review meetings, resolving data discrepancies, managing data entry quality, and ensuring data consistency and accuracy. The ability to interpret complex protocols and translate them into robust data management systems is essential. As a remote-first position, exceptional communication, organizational, and self-management skills are paramount. You will need to proactively engage with teams across different time zones and maintain strong working relationships without direct physical proximity. We are looking for a strategic thinker who can contribute to process improvements and mentor junior data management staff. A minimum of 8 years of progressive experience in clinical data management within the pharmaceutical or biotech industry is required. A Bachelor's or Master's degree in a scientific or related field is preferred. Proficiency in Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical) and familiarity with CDISC standards are mandatory. This is an exceptional opportunity to make a significant impact on the development of life-saving medicines from the comfort of your home office, contributing to groundbreaking research and development initiatives for our client.

A leading pharmaceutical research organization is seeking a highly skilled Principal Clinical Data Manager for their operations in Sheffield, South Yorkshire, UK . This role is pivotal in ensuring the integrity, accuracy, and quality of clinical trial data. You will be responsible for overseeing all aspects of clinical data management, from database design and setup to data validation, cleaning, and database lock. Your expertise will ensure compliance with regulatory requirements and company standards.

Key responsibilities include developing clinical data management plans, creating data validation specifications, and managing external vendors involved in data management activities. You will lead and mentor a team of data managers, providing guidance and support to ensure efficient and effective data collection and processing. The ideal candidate will possess a Bachelor's or Master's degree in a scientific or healthcare-related field, with a minimum of 8 years of experience in clinical data management, including significant experience in a leadership or principal role. A strong understanding of clinical trial processes, CDISC standards (SDTM, ADaM), and various EDC systems (e.g., Medidata Rave, Oracle Clinical) is essential. Excellent analytical, problem-solving, and communication skills are required, along with meticulous attention to detail. Experience with database programming and query writing is highly desirable. This is an excellent opportunity to contribute to critical drug development programs and advance your career in a highly respected pharmaceutical organization.

Our client is seeking a highly experienced and meticulous Senior Clinical Data Manager to join their dynamic pharmaceutical research team. This role plays a critical part in ensuring the integrity, accuracy, and reliability of clinical trial data, which is essential for regulatory submissions and drug development. You will be responsible for overseeing the design, development, and execution of clinical databases, managing data entry processes, and ensuring compliance with all relevant data management standards and regulatory guidelines (e.g., ICH GCP). The Senior Clinical Data Manager will lead data management activities across multiple clinical trials, collaborating closely with clinical operations, biostatistics, and medical coding teams. Key responsibilities include developing data management plans (DMPs), creating case report forms (CRFs), establishing data validation checks, and performing data cleaning activities. You will also manage user acceptance testing (UAT) for clinical databases and work with external vendors as needed. This position requires a strong understanding of clinical trial processes, database technologies (e.g., EDC systems like Medidata Rave, Oracle Clinical), and data quality principles. The ideal candidate will possess excellent analytical and problem-solving skills, with a keen eye for detail and a commitment to data accuracy. Leadership potential and the ability to mentor junior data managers are highly valued. While this role offers a hybrid work arrangement, flexibility to attend key meetings on-site in Liverpool will be expected. You will contribute significantly to the successful execution of clinical studies, ensuring that high-quality data supports critical research outcomes.

Responsibilities:

• Develop and implement comprehensive Data Management Plans (DMPs) for clinical trials.
• Design, build, and maintain clinical databases using Electronic Data Capture (EDC) systems.
• Oversee the creation and validation of Case Report Forms (CRFs) and data entry guidelines.
• Establish and execute data validation procedures, including query generation and resolution.
• Ensure data accuracy, completeness, and consistency throughout the clinical trial lifecycle.
• Perform data review and cleaning activities in accordance with protocols and DMPs.
• Manage User Acceptance Testing (UAT) for clinical databases and related systems.
• Collaborate with cross-functional teams, including biostatistics, clinical operations, and regulatory affairs.
• Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and other relevant regulations.
• Contribute to the development and maintenance of standard operating procedures (SOPs) for data management.
• Act as a subject matter expert for clinical data management within the organisation.
• Mentor and provide guidance to junior clinical data management personnel.

Qualifications:

• Bachelor's degree in a life science, computer science, or related field.
• Minimum of 5 years of experience in clinical data management within the pharmaceutical or biotech industry.
• Proven experience with EDC systems (e.g., Medidata Rave, Oracle Clinical, Veeva).
• Strong understanding of ICH-GCP guidelines and regulatory requirements for clinical data.
• Excellent knowledge of database design, data validation, and data cleaning processes.
• Proficiency in clinical trial methodologies and terminology.
• Strong analytical and problem-solving abilities with meticulous attention to detail.
• Effective communication and interpersonal skills, with the ability to work collaboratively in a hybrid team environment.
• Experience in leading data management activities for multiple studies is advantageous.

Our client, a leading pharmaceutical research organization, is seeking a Principal Clinical Data Manager to join their globally distributed team. This is a fully remote position, offering the flexibility to work from anywhere while contributing to critical pharmaceutical development projects. You will be responsible for overseeing the design, development, and implementation of clinical databases, ensuring data integrity, accuracy, and compliance with regulatory standards. This senior role requires extensive experience in clinical data management, a deep understanding of CDISC standards, and strong leadership capabilities. You will play a crucial role in the success of clinical trials, ensuring that data is managed efficiently and effectively to support regulatory submissions and therapeutic advancements.

Key Responsibilities:

• Lead the design, setup, and maintenance of clinical databases according to study protocols and therapeutic area requirements.
• Develop and implement data management plans (DMPs), edit check specifications, and data validation procedures.
• Oversee data cleaning activities, issue resolution, and database lock processes for clinical trials.
• Ensure compliance with Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and other relevant regulatory requirements.
• Develop and maintain standard operating procedures (SOPs) and work instructions for clinical data management.
• Provide technical expertise and guidance on clinical data management best practices.
• Mentor and train junior data managers and data management staff.
• Act as a key point of contact for data management activities, collaborating with clinical operations, biostatistics, programming, and medical teams.
• Participate in the selection and implementation of data management technologies and tools.
• Conduct quality control checks and audits to ensure data accuracy and consistency.
• Contribute to the development of integrated data management strategies across multiple projects and therapeutic areas.
• Review and approve data management-related documents, including CRFs, database specifications, and validation reports.
• Proactively identify risks and issues related to data management and implement mitigation strategies.
• Stay current with industry trends, regulatory changes, and advancements in clinical data management.

Required Qualifications:

• Bachelor's degree in a scientific, technical, or health-related field. Master's degree preferred.
• Minimum of 10 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry.
• Extensive knowledge of clinical trial processes and regulatory requirements (GCP, ICH, FDA).
• Proficiency in CDISC standards (SDTM, ADaM) and experience with data warehousing solutions.
• Strong experience with clinical data management systems (e.g., Medidata Rave, Oracle Clinical, SAS).
• Proven ability to lead data management activities for complex, global clinical trials.
• Excellent understanding of database design, data validation techniques, and data cleaning processes.
• Strong leadership, project management, and problem-solving skills.
• Exceptional communication, presentation, and interpersonal skills.
• Ability to work independently and collaboratively in a remote team environment.
• Experience in mentoring and developing data management professionals.

This fully remote role offers a significant opportunity to influence drug development and advance your career at the forefront of pharmaceutical innovation.

This is a fully remote opportunity for a skilled Clinical Data Manager to join a leading global pharmaceutical research organization. Our client is at the forefront of developing life-changing therapies and seeks a dedicated professional to manage and oversee clinical trial data from study start-up through database lock. You will be responsible for developing Data Management Plans (DMPs), designing Case Report Forms (CRFs), and establishing data validation checks and edit specifications in accordance with protocol requirements and regulatory guidelines (e.g., ICH GCP). This role involves leading data cleaning activities, ensuring the accuracy, completeness, and integrity of clinical trial data. You will collaborate closely with biostatisticians, clinical research associates (CRAs), study managers, and external vendors to resolve data discrepancies and queries in a timely manner. Database validation and User Acceptance Testing (UAT) will be key responsibilities, ensuring the clinical database meets all functional and data integrity requirements. You will also contribute to the development and maintenance of data management SOPs and work instructions. A strong understanding of CDISC standards (SDTM and ADaM) and EDC systems (e.g., Medidata Rave, Oracle InForm) is essential. Experience in managing data for Phase I-IV clinical trials across various therapeutic areas is highly desirable. The ideal candidate will possess a Bachelor's degree in a scientific discipline, computer science, or a related field, with a minimum of 5 years of experience in clinical data management within the pharmaceutical or biotechnology industry. Exceptional attention to detail, strong organizational skills, and the ability to manage multiple projects simultaneously are crucial. Excellent communication and interpersonal skills are necessary for effective remote collaboration. This is a remote-first position, offering the flexibility to work from anywhere within the UK, with regular virtual team meetings and collaboration. If you are a proactive and experienced Clinical Data Manager looking for a challenging and rewarding remote role, we encourage you to apply.

Our client, a pioneering biopharmaceutical company dedicated to developing innovative therapies, is seeking a highly skilled Lead Clinical Data Scientist to drive advancements in their drug discovery and development programs. This key role, based in the vibrant city of Edinburgh, Scotland, UK , will involve leading a team of data scientists in the analysis of complex clinical trial data to generate actionable insights that inform strategic decision-making. You will leverage statistical modeling, machine learning, and data visualization techniques to unlock the full potential of our client's rich datasets.

Key responsibilities will include:

• Leading and mentoring a team of clinical data scientists, fostering a collaborative and high-performance environment.
• Developing and applying advanced statistical and machine learning methodologies to analyze clinical trial data.
• Designing and implementing data analysis plans to address key research questions and objectives.
• Interpreting complex data findings and communicating insights effectively to clinical, research, and regulatory teams.
• Ensuring the accuracy, integrity, and reproducibility of all data analysis and reporting.
• Collaborating with biostatisticians, clinicians, and IT professionals to integrate data sources and enhance analytical capabilities.
• Contributing to the development of predictive models for patient response, disease progression, and treatment efficacy.
• Staying current with the latest advancements in data science, clinical research, and relevant therapeutic areas.
• Overseeing the development and maintenance of data analysis tools and platforms.
• Contributing to regulatory submissions and scientific publications.

The ideal candidate will possess a PhD or Master's degree in Statistics, Data Science, Biostatistics, Computer Science, or a related quantitative field, with a minimum of 7 years of progressive experience in clinical data analysis, including at least 3 years in a leadership or team management capacity. Proven experience in applying statistical modeling and machine learning techniques to large-scale clinical trial datasets is essential. Strong programming skills in R or Python, experience with data visualization tools (e.g., Tableau, Power BI), and familiarity with clinical data standards (e.g., CDISC) are required. Excellent communication, presentation, and interpersonal skills are paramount for effective collaboration and leadership. This role offers a competitive salary, attractive benefits, and the opportunity to make a significant impact on the development of life-saving medicines.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Data Analytics & Computational Sciences
**Job Sub** **Function:**
Data Governance & Policy
**Job Category:**
Professional
**All Job Posting Locations:**
High Wycombe, Buckinghamshire, United Kingdom
**Job Description:**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at ( are searching for the best talent for a **Manager Clinical Data Transparency, Clinical Registry** within our Integrated Data Analytics and Reporting (IDAR) team, located **High Wycombe, United Kingdom.** This role is Hybrid
**Purpose:**
The Manager, Clinical Data Transparency, serves as an individual contributor and emerging subject matter expert in Data Transparency (DT), working independently with minimal supervision. This role involves consulting on projects, programs, and processes that span multiple related areas to support the organisation's overall DT strategy. The Manager applies in-depth DT knowledge to maintain and improve best-in-class policies, procedures, and plans for clinical registries, data and document anonymisation, data sharing, and plain language summaries.
Are you ready to join our team? Then please read further!
**You will be responsible for:**
+ Acting as a top-level specialist to establish programs and new initiatives for the organisation to advance DT priorities.
+ Managing projects, programs or processes for the DT area.
+ Understanding, communicating and ensuring adherence to DT and data anonymisation policies.
+ Governing DT capabilities and roadmap, including strategic priorities for DT.
+ Reviewing critical quality issues to drive root cause assessment and mitigation planning.
+ Studying regulatory and industry trends in data transparency and anonymisation to integrate trends and best practices.
+ Coaching and training junior colleagues in techniques, processes and responsibilities.
+ Integrating J&J Credo and Leadership Imperatives into team goals and decision-making.
The Manager Clinical Data Transparency, Clinical Registry:
+ Is the owner of the overall integrity of the compliance management system for country specific clinical trial registries (including EU-PASS and the Pan-African CTR) and ensures consistent use by the clinical registry, vendor's disclosure associates and business partners.
+ Is subject matter expert on local clinical trial registries, and as such provides expertise in discussions and projects with internal and external business partners
+ Is responsible for the country specific clinical trial registry process
+ Writes, trains and maintains job aids for local clinical trial registries where needed in addition to the company SOPs.
+ Ensures service level agreements between the clinical registry and countries and business partners are made
+ Reports and analyses metrics on the country specific registry process
+ Oversees vendors for outsourced activities
+ Assigns the country portfolio to the CRG
+ Assigns countries to clinical registry administrators
+ Manages the process and deliverables through individual and team meetings and ensure consistency and continuation of process and policy
+ May manage one of the other key disclosure processes
+ In joint meetings with the other Clinical Registry Managers develops a good understanding of all registry activities and can provide guidance and backup in the team
**Principal Relationships:**
**Internal:** Align, collaborate, advise, and share best practices with other functions and teams in Therapeutic Areas, Global Development, Regulatory Affairs, Data Sciences, Legal, Global Privacy, Data Transparency and others as needed.
**External:** Interact and collaborate with vendors.
Act as J&J representative for defining process standards and sharing practices with industry counterparts and working groups, as required.
**Education and Experience Requirements:**
+ A bachelor's degree in a scientific, technology or healthcare discipline, or equivalent experience
+ At least 5 years of relevant pharmaceutical/scientific experience in a related discipline; e.g. medical writing, data management, biostatistics, clinical programming, clinical trials operations is required!
+ Excellent understanding of at least one of the following: regulatory clinical trial disclosure requirements, translation of scientific content for a lay audience, anonymisation of clinical data and documents, data sharing.
+ Demonstrated written and verbal communications skills
+ Demonstrated customer focus and solution-oriented experience
+ Demonstrated interpersonal skills to build relationships with internal and external business partners
+ Demonstrated leadership on cross-functional projects within a matrix organisation
+ Demonstrated leadership in decision making and problem solving
**Benefits:**
We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organization.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will be considered for employment without regard to any other characteristic protected by law.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform important job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
#LI-Hybrid

Clinical Data Engineer (Client dedicated)
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 will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
In this role, you will lead the design, development, and implementation of enterprise-level data pipelines that support clinical trial data integration and analysis. This role is instrumental in ensuring the efficient ingestion, transformation, and delivery of high-quality clinical data across multiple systems and sources to enable data-driven insights, regulatory compliance, and business excellence.
**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 maximise savings and plan with confidence for the years ahead
+ Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: 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, colour, 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 through the form below.
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.
**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 ( 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