Jobs at ICON plc

Lead strategy, roadmap, and delivery for multiple enterprise healthcare products. Drive discovery, prioritize backlog, partner with engineering and stakeholders, measure outcomes, and optimize product performance in regulated clinical research environments.

Design, validate, and maintain programming solutions for clinical trial data analysis and reporting. Generate statistical datasets, tables, listings, and figures for regulatory submissions. Collaborate with data scientists and biostatisticians, enforce coding standards and data quality controls, mentor colleagues, and adopt new programming and data-management tools to improve efficiency.

Manage clinical trial operations, ensuring adherence to timelines and quality standards. Collaborate with teams, build relationships with investigators, and maintain compliance with regulations.

The Informed Consent Specialist develops, reviews, and ensures compliance of informed consent forms for clinical trials while collaborating with stakeholders and managing timelines.

Manage and coordinate investigator payments for clinical trials: review invoices, verify accuracy and contract compliance, resolve payment queries with clinical and finance teams, maintain financial records for audits, streamline payment processes, and communicate payment procedures with investigators and sites.

The Software Engineering Manager will lead the development of technology solutions for clinical trial operations, manage software delivery, mentor engineers, and ensure compliance with healthcare regulations.

As a Senior Clinical Data Coordinator, you will design and analyze clinical trials, manage data flow, and mentor junior coordinators while ensuring compliance with standards.

Senior EUC/Operations Engineer responsible for designing, operating, and improving enterprise endpoint and VDI platforms (Intune, MECM/SCCM, Citrix, Jamf). Lead incident resolution, define secure baselines, use operational KPIs, manage complex changes, produce runbooks/reports, strengthen endpoint security, collaborate cross-functionally, mentor junior engineers, and participate in on‑call support.

Lead clinical data management across trials ensuring data integrity, regulatory compliance, inspection readiness, and delivery of CRFs, datasets, and review plans. Collaborate with cross-functional teams and vendors, define eCRF/data requirements, provide team leadership, training, and continuous improvement.

Lead financial business partnering by managing budgeting, forecasting, and analysis for departments and projects. Provide strategic insights, prepare reports for stakeholders, identify cost-savings, and build cross-functional relationships while developing and overseeing a finance team.

Responsible for processing and payment of invoices, reconciliation of accounts, and resolution of supplier and employee queries.

Drive new and repeat business for ICON's Phase II-III clinical services across pharmaceutical, biotech, and medical device clients in India. Build and maintain client relationships, support proposal development and bid defense, collaborate cross-functionally, identify market opportunities, and contribute to strategic global growth initiatives.

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 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.

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

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.

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.