Jobs at ICON plc

Senior-level network engineer providing highest-tier escalation for global network operations. Lead troubleshooting, major incident recovery, root-cause analysis, network design and delivery for enterprise projects, datacenter/cloud connectivity, security compliance, and automation across multi-vendor environments (Cisco ACI, Fortinet, F5, SD-WAN, Azure/AWS). Mentor junior engineers and support 24x7 mission-critical operations.

Administer and support enterprise Citrix environment (Virtual Apps & Desktops, StoreFront, Director, Delivery Controllers, MCS). Manage patching and lifecycle, handle incidents/escalations, perform root cause analysis, optimize performance, document operations, implement changes, and resolve issues escalated from EUS and other teams.

Support the Investigator Payments team with setup, maintenance, and execution of investigator payments. Serve as a contact for payment inquiries, liaise with clinical teams and internal departments to resolve issues, and help improve IPG systems and processes to ensure accurate, timely payments per investigator contracts.

Support clinical data management by maintaining eCRFs, data validation specs, and study procedures; reconcile clinical and third-party data; track study metrics; address and resolve data issues; communicate status to project teams.

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.

Support clinical data management activities including eCRF maintenance, data validation spec creation, third-party data reconciliation, tracking study metrics, addressing data queries, and identifying root causes to resolve data issues.

Lead statistical strategy and execution for Phase I-III oncology trials. Review protocols, SAPs, and clinical reporting for scientific and regulatory quality. Provide client-facing statistical guidance, perform and oversee analyses using SAS and/or R, contribute to proposals and presentations, mentor junior statisticians, and drive process improvements.

Lead development and validation of SAS programs for clinical trial statistical analysis and reporting. Collaborate with biostatisticians on analysis plans, perform QC on outputs, prepare statistical reports for regulatory submissions, and drive programming process improvements.

Negotiate, execute, and manage clinical trial agreements and site budgets; support site start-up and regulatory submissions; track timelines and risks; ensure compliance and documentation; mentor junior staff; and drive process improvements to support timely site activation.

Lead global Study Start-Up and site activation efforts: develop and execute SSU strategy and plans, manage regulatory/ethics submissions, oversee site contracts and budgets, drive milestones to IP release, maintain CTMS/eTMF documentation, coordinate cross-functional stakeholders, mitigate risks, and report progress to sponsors and leadership.

Lead and deliver IT projects and programmes for the organisation: develop and execute project plans, manage cross-functional teams, define scope with stakeholders, mentor team members, produce project documentation and reports, integrate best practices and emerging technologies, and contribute to strategic planning and organisational growth.

Execute data-driven site identification and qualification for clinical studies: conduct feasibility outreach, assess site capabilities and patient access, manage start-up documentation, maintain tracking tools, collaborate with feasibility and project teams, and improve site selection processes. Role requires working US shift (8 PM–5 AM IST).

Lead design, development, and validation of clinical data programming solutions. Collaborate with biostatisticians and data managers to produce and validate datasets, tables, listings, and figures (TLFs), ensure data accuracy and regulatory compliance (SDTM/ADaM), perform quality control, and mentor junior programmers while managing multiple projects.

Deliver clinical data management tasks including eCRF and validation spec maintenance, clinical and third-party data reconciliation, tracking study metrics, addressing data queries, and identifying root causes to resolve data issues while collaborating with multidisciplinary teams.

Provide 24/7 Linux system administration and production support for RHEL/CentOS/Oracle Linux environments. Monitor performance, patch systems, troubleshoot incidents, perform RCA, automate operations (Bash/Python), support IaC/CI-CD initiatives, collaborate across storage/middleware/database/network teams, maintain documentation, enforce security and ITIL-aligned processes.

Negotiate and execute clinical trial site contracts and budgets for APAC studies, manage a contracts portfolio, liaise with legal/finance/project teams, maintain negotiation records, resolve contractual issues, and support template/process improvements while mentoring junior staff as needed.

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.

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

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.