ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior Clinical Data Science Lead at ICON, you will lead the analysis, interpretation, and management of clinical data to drive the success of our clinical trials.
What You Will Do:You will oversee clinical data science workstreams, ensuring deliverables meet quality and timeline expectations while acting as the functional lead across multiple low to moderately complex studies.
Key responsibilities include:
- Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, data review, and reporting.
- Leading multiple low/moderately complex studies as the functional Clinical Data Science Lead and acting as a resource for colleagues with less experience.
- Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs.
- Overseeing the analysis and review 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.
- Applying project management skills to proactively manage timelines, resource requirements, and financial tracking.
- Developing a detailed understanding of protocol content and interpreting critical data and data review requirements.
- Reacting and adapting requirements, processes, and timelines in an agile manner to meet project and business needs.
- Tracking study progress and keeping functional management and project management informed of issues that may affect project target dates, scope, or budget, escalating risks in a timely manner.
- Working independently and with other project leads, as needed, to negotiate timelines and key deliverables with clients, external customers, and internal departments.
- Understanding project-level revenue recognition and forecasting processes, providing input on actual and forecasted units/hours (revenue and resources) to the Clinical Data Science Project Manager.
- Undertaking other responsibilities as assigned.
You will have solid clinical data science experience, with the ability to manage competing priorities, lead multiple studies, solve complex problems, and support the development of your team.
Required qualifications and experience:
- Bachelor's degree in life sciences, computer science, or a related discipline.
- Typically 5–8 years of experience in Clinical Data Science, Clinical Data Management, or a related field. An equivalent combination of education, training, and relevant experience may be considered in place of the stated education and experience.
- Extensive experience in clinical data science, with a strong focus on clinical data management, data review, and analysis in clinical trials.
- Enhanced knowledge of clinical data management, clinical data science, and clinical data review activities.
- Applied project management skills, including experience managing timelines, resource requirements, and financial tracking.
- Detailed understanding of protocol content and interpretation of critical data and data review requirements.
- Strong leadership skills and a proven ability to lead multiple studies, manage cross-functional teams, and act as a resource for colleagues with less experience in a fast-paced, matrix environment.
- Strong problem-solving skills with the ability to analyse and investigate complex issues, identify solutions that are not readily apparent, and anticipate future challenges.
- Ability to work independently, establish approaches, and lead resources to achieve operational and strategic objectives with impact on medium-term goals.
- Expertise in data analysis tools, statistical software, and data visualization techniques.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to adapt communication style, influence stakeholders, present and defend complex analyses, and secure approval on complex matters
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
Skills Required
- Bachelor's degree in life sciences, computer science, or related discipline (or equivalent combination of education, training, and experience)
- Typically 5-8 years of experience in Clinical Data Science, Clinical Data Management, or a related field
- Extensive experience in clinical data management, data review, and analysis in clinical trials
- Enhanced knowledge of clinical data management, clinical data science, and clinical data review activities
- Applied project management skills, including managing timelines, resource requirements, and financial tracking
- Detailed understanding of protocol content and interpretation of critical data and data review requirements
- Strong leadership skills with experience leading multiple studies and managing cross-functional teams
- Strong problem-solving skills and ability to analyze and investigate complex issues
- Ability to work independently, establish approaches, and lead resources to achieve operational and strategic objectives
- Expertise in data analysis tools, statistical software, and data visualization techniques
- Excellent communication, interpersonal, and stakeholder management skills
ICON plc Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.
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Healthcare Strength — Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
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Leave & Time Off Breadth — Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
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Retirement Support — Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.
ICON plc Insights
What We Do
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.






