Jobs at ICON plc

Lead and coordinate clinical research projects: develop and manage plans, timelines, budgets, and resources; lead cross-functional teams; monitor progress and risks; engage stakeholders; prepare and present status reports to senior management.

Monitor early-stage (Phase I) clinical trials: conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; resolve data queries; collaborate with investigators and prepare/review study documentation including protocols and clinical study reports.

Perform onsite and remote clinical trial monitoring activities including site initiation, routine and close-out visits; coordinate study setup, maintain documentation, manage queries, review medical data for ICH-GCP compliance, liaise with investigators and site staff, and support feasibility and study documentation.

Lead teams delivering feasibility assessments and site activation for global clinical trials. Manage start-up strategies, regulatory/contract submissions, feasibility data review, stakeholder collaboration for proposals, monitor performance metrics, and coach FSA staff to drive continuous improvement and predictable study start-up.

Lead and support development of high-quality clinical trial proposals by gathering input from cross-functional teams, preparing and reviewing proposal content and formatting, coordinating subject matter experts, tracking timelines, and mentoring junior colleagues to ensure timely, compliant RFP submissions.

Lead clinical trial operations and delivery across global programs: oversee budgets, develop monitoring plans, train and mentor CRAs, drive study start-up and enrollment, manage vendors and sponsor relationships, review trip reports and implement CAPAs.

Lead risk-based study management for assigned clinical trials, maintaining study-level risk assessments, facilitating cross-functional risk reviews, reviewing centralized monitoring outputs and KPIs, driving mitigation plans, supporting escalation and root-cause analysis, and ensuring inspection-ready, defensible oversight aligned with sponsor expectations.

Lead global portfolio-level resource demand and capacity planning for clinical delivery groups. Own forecasting, challenge resource requests, optimize utilisation and bench management, lead and develop the resource management team, partner cross-functionally (Finance, PM, TA, Sales), advance forecasting tools and governance, ensure compliance with ICH-GCP and quality standards, and provide strategic guidance to protect delivery quality and margin.

Perform site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; review data and resolve queries; collaborate with site staff and contribute to study documentation and reports.

The role involves monitoring supplier performance, ensuring compliance, developing supplier relationships, and managing data quality for clinical trials.

As Project Manager, FSA, you will oversee site selection and activation, ensuring project goals are met within budget and timelines, while collaborating with internal and sponsor teams. You will manage site activation activities, maintain quality standards, and act as the customer contact for assigned studies, contributing to business development efforts and ensuring compliance.

The Statistical Programmer II develops, validates, and executes statistical programs for clinical trial data analysis while mentoring junior programmers and collaborating with biostatisticians.

The Manager, Clinical Operations will oversee clinical trials, ensure compliance with regulations, mentor staff, and build stakeholder relationships to enhance operational efficiency.

Monitor clinical trials through site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; review and resolve data queries; collaborate with investigators and site staff; and contribute to study documentation and clinical study report preparation.

Manage day-to-day clinical trial operations including planning, protocol implementation, vendor and investigator management, regulatory compliance, risk management, timelines, budgets, and team development to deliver high-quality trial outcomes.

Serve as primary ICON liaison to investigator sites, build strong long-term relationships, support multiple studies, align site capabilities with study needs, monitor site performance and metrics, drive improvements, and contribute to site engagement strategies and process enhancements.

Conduct site setup and monitoring activities for clinical trials, maintain study documentation and reports, resolve sponsor queries, review study documentation and feasibility, ensure protocol and regulatory compliance, maintain stakeholder and site relationships, and support patient safety.

Lead onsite and remote monitoring for oncology clinical trials, ensuring data integrity, subject safety, TMF reconciliation, regulatory readiness, site activation, training, KRI monitoring, CAPA implementation, and site relationship management.

Lead client relationships and sales for CRO/RWE services: manage full sales cycle, identify expansion opportunities, coordinate cross-functional delivery, monitor account performance, and mentor colleagues to drive revenue and retention.

Accountable for end-to-end country-level trial delivery for oncology and multi-therapeutic studies: vendor and vendor PO management, local milestones, resourcing, inspection readiness, cross-functional coordination with LTMs/LSMs/CTAs/SCMs, reporting to Functional Manager and Global Trial Leader, and supporting documentation, training, and ad hoc country-level issue resolution.