Jobs at ICON plc

Prepare monthly financial and management accounts for multiple entities; maintain trial balance and balance sheet reconciliations; calculate cost-plus revenue; ensure local statutory filings (VAT, CT) and SOX compliance; monitor weekly cash flow; liaise with local advisors and auditors; assist with forecasts, budgets, and Finance Manager requests.

Lead clinical delivery for studies including budget oversight, monitoring plan development, CRA training and mentoring, driving study start-up and enrollment, risk mitigation, stakeholder management, and clinical reporting to ensure study timelines and integrity.

Lead and manage clinical external data activities: author and track Data Transfer Specifications (DTS), ensure CDISC-compliant data structures, reconcile and harmonize external datasets, oversee vendor data delivery, support eCRF/EDC builds, train teams on DTS use, and contribute to process improvements and regulatory-compliant analytics for clinical trials.

Lead RBQM activities across study setup and maintenance: author RBQM plans, identify and document critical-to-quality data/processes, facilitate and ensure timely risk assessments, review critical data flows and monitoring strategies (T-SDV/T-SDR, SDV/SDR), define QTLs/KRIs, run quarterly operational quality reviews (QRRM), trend CAPAs/non-conformances, and report findings to governance while serving as an escalation point.

Lead development and maintenance of Data Transfer Specifications, manage clinical external data delivery, ensure CDISC compliance, support data reconciliation, oversee vendor data management, train teams, review eCRF/EDC impacts, and ensure regulatory adherence for biomarker, imaging, and eCOA data.

Deliver clinical data management tasks including eCRF maintenance, data validation/specifications, reconciliation with third-party sources, tracking study metrics, resolving data queries, and identifying root causes to improve data quality.

Design, configure, integrate, and test clinical systems aligned with study protocols. Lead system enhancements, mentor colleagues, drive process improvements, advise on technology adoption, and stay current with clinical tech trends to optimize trial metrics and user experience.

Design, maintain, and analyze clinical trial data and eCRFs. Support Data Management Study Lead with validation specs and procedures, reconcile clinical and third-party data, track study metrics, resolve data issues, and liaise with cross-functional teams to ensure data quality and compliance.

Prepare and analyze financial statements, execute month- and year-end closes, perform reconciliations and variance analysis, ensure compliance and support audits, develop financial models for budgeting/forecasting, collaborate cross-functionally, and mentor junior accounting staff to ensure accurate financial operations.

Designs and performs risk-based clinical data review and cleaning across trials. Plans and coordinates data review, creates review checks and dashboards, liaises with programmers and trial partners, raises and resolves queries, ensures regulatory compliance, and supports audits and process improvements.

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.

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.

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.

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.

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.