Jobs at ICON plc

Director, IT based in Chennai (hybrid, office-based). Senior IT leader responsible for overall IT strategy, operations, infrastructure, security, vendor management, team leadership, and alignment of IT with business needs within the clinical research organization.

Process accurate and timely employee payroll, maintain payroll records, deductions, earnings, and tax documentation, respond to payroll inquiries, resolve discrepancies, collaborate with HR and Finance on data integrity, and support payroll reporting and analysis.

Leads clinical data science activities for clinical trials, including data management strategy, data integration, analysis, reporting, governance, quality control, and regulatory compliance. Oversees workstreams, ensures timely and high-quality deliverables, provides strategic guidance, collaborates with cross-functional stakeholders, and develops teams. Requires approximately 15% travel.

As a Clinical Data Science Programmer, you will develop and validate programming code for clinical trials, ensuring data integrity and compliance with regulatory standards while collaborating with scientists and statisticians.

The Manager, Statistical Programming leads a team in developing and validating statistical analysis solutions for clinical trials while ensuring quality and regulatory compliance.

The role involves developing and validating statistical programs for clinical trials, collaborating with teams on analysis, and mentoring junior programmers.

The Logistics Analyst will analyze logistics data, optimize supply chain processes, collaborate with teams and vendors, and report on performance metrics.

The Database Developer II will design and maintain databases for clinical research projects, optimize data processes, and troubleshoot database issues.

The Senior Biostatistician will lead statistical analyses for clinical trials, mentor junior team members, and manage client interactions while ensuring compliance with regulatory standards.

Design, develop, deploy, and maintain scalable enterprise applications using ReactJS front-ends and ASP.NET Core APIs. Implement cloud-native solutions (Azure/AWS), microservices, CI/CD/DevOps, containerization, testing, and performance optimization while collaborating with cross-functional teams.

Lead vision, roadmap, and outcomes for multiple enterprise products. Drive discovery, prioritize backlogs, partner with engineering and cross-functional teams, monitor performance, and deliver business impact in a regulated healthcare environment.

Design, develop, and maintain scalable software to support clinical trial operations and data management. Collaborate with product, design, and engineering teams to translate requirements into technical solutions, perform code reviews, troubleshoot complex issues, and improve development processes while keeping up with emerging technologies.

Analyze and improve engineering systems and processes, design and validate models and simulations, develop and maintain database objects and APIs, support cloud deployments and CI/CD, collaborate with cross-functional teams, participate in code reviews, troubleshooting, and Agile development.

Design, implement, and deploy advanced data models and machine learning algorithms on large clinical or enterprise datasets. Perform statistical analyses, mentor colleagues, collaborate with cross-functional teams, and communicate insights to inform strategic decisions and process improvements.

Lead clinical data management activities: create/maintain data management plans, resolve data discrepancies, collaborate with cross-functional teams, mentor junior coordinators, and support study documentation to meet timelines and regulatory standards.

Provide application support for pharmacovigilance systems (Argus and related platforms): user and product setup, generate validated and ad-hoc safety listings, troubleshoot E2B/ICSR transmissions, support releases, collaborate with IT/PVSS and vendors, and respond to audit and regulatory inspection requests.

Support financial planning, analysis, and reporting including budgets, forecasts, month-/year-end close, account reconciliations, variance analysis, cross-functional financial tracking, and development of financial models and tools to inform decision-making.

Support clinical trial program operations by developing project plans, timelines, and budgets; provide operational guidance; collaborate cross-functionally; monitor trial progress; identify and implement process improvements to ensure efficient, compliant trial execution.

Designs and analyzes clinical trial data, maintains eCRFs and validation specs, reconciles clinical and third-party data, tracks study metrics, resolves data issues, and supports cross-functional teams to ensure data quality and regulatory compliance.

Lead development, implementation, and governance of clinical data standards (CDISC/CDASH/Controlled Terminology). Provide subject-matter expertise, mentor staff, support sponsors, develop training and documentation, and drive standards adoption across clinical data management. Advise on compliance and continuous improvement; lead projects and cross-functional initiatives. Travel ~15%.