Jobs at ICON plc

Leads the strategic and tactical management of an Imaging Project Management team within clinical research. Responsibilities include supervising project managers and assistants, allocating resources, managing workloads and forecasts, developing performance metrics, resolving escalations, improving processes, overseeing training and compliance, supporting recruitment, managing financial performance, and leading risk and contingency planning. Requires up to 25% travel.

Manage feasibility and site activation activities for clinical studies, including project plans, timelines, site recommendations, regulatory and ethics submissions, essential documents, contracts, and activation milestones. Coordinate cross-functional and sponsor stakeholders, track KPIs, mitigate risks, resolve study issues, support audits and inspections, and ensure quality, budget, and timeline compliance. The role also includes mentoring, process improvement, business development support, and approximately 10% domestic or international travel.

Conduct clinical trial site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and support study documentation. Requires oncology monitoring experience, clinical trial expertise, strong organization and communication skills, and willingness to travel up to 60%–75% within the assigned region.

Conduct clinical trial site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review data and resolve queries; and support preparation of protocols and clinical study reports. Requires oncology monitoring experience, clinical trial regulatory knowledge, strong organization and communication skills, and regional travel of up to 60–75%.

Conduct site selection, initiation, monitoring, and close-out visits for clinical research studies. Serve as the sponsor-site contact, ensure ICH-GCP and regulatory compliance, maintain CTMS and eTMF documentation, monitor patient safety and drug accountability, support recruitment and retention, resolve data queries, track site progress and payments, and escalate risks while collaborating with clinical trial partners.

Lead feasibility informatics strategy for clinical trial proposals and awarded feasibility projects. Provide data-driven feasibility analyses using internal/external data, support bid defenses, manage delivery and handover to site identification, assess risks, and collaborate with cross-functional teams to meet sponsor objectives.

The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

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.

Lead site management and monitoring for oncology clinical trials, ensuring data integrity, subject safety, inspection readiness, and regulatory compliance. Perform on-site and remote monitoring, train and mentor CRAs, manage TMF/essential documents, drive site activation and engagement, and implement CAPA and KRI oversight.

Lead on-site clinical monitoring for oncology/hematology trials: conduct site selection, initiation, routine and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor patient safety and AE/SAE reporting; oversee drug accountability, support recruitment and retention, resolve data queries, track site budgets, and escalate risks to clinical teams while collaborating cross-functionally.

Serve as primary contact between investigational sites and sponsor to conduct site selection, initiation, routine monitoring, and close-out. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety (AE/SAE/PQC), support recruitment and drug accountability, resolve data queries, track site training and budgets, escalate risks, and collaborate with cross-functional clinical teams.

Oversee Phase I oncology clinical trial monitoring for sponsor-dedicated studies. Conduct site visits, ensure protocol and regulatory compliance, assess site performance, resolve issues, support data integrity, train site staff and CRAs, and collaborate with cross-functional stakeholders to maintain successful trial execution.

Program and manage real-world healthcare datasets from claims and EMR sources. Clean, transform, normalize, and prepare analysis-ready data; create data dictionaries and programming documentation; build dashboards; and support research teams with analytics and programming for real-world evidence generation.

Manages multiple healthcare improvement initiatives across timelines, budgets, workstreams, risks, deliverables, and stakeholder relationships. Coordinates Medical Affairs, Legal, compliance, health systems, professional societies, research institutes, and other partners. Tracks spending and milestones, supports governance meetings, synthesizes performance data, maintains project dashboards and collaboration tools, conducts landscape analyses, and identifies process improvements. Requires healthcare systems knowledge, quality improvement exposure, and CRO or pharma project management experience.

Conduct clinical trial site qualification, initiation, monitoring, and close-out visits for HemOnc studies. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review data and resolve queries; and support study documentation, protocols, and clinical study reports. Requires oncology monitoring experience, strong clinical trial knowledge, and willingness to travel 60–75% regionally.

Conduct clinical trial site qualification, initiation, monitoring, and close-out visits for oncology studies. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and support preparation and review of study documentation. Requires at least two years of Clinical Research Associate experience, oncology monitoring experience, scientific or healthcare education, ICH-GCP knowledge, and willingness to travel 60–75% within the region.

Leads clinical outcome assessment (COA) research programs, including PRO, ClinRO, PerfO, and ObsRO development and validation. Designs qualitative and psychometric research, supports clinical trial protocols and statistical plans, prepares regulatory documents, develops COA strategies, and publishes findings. Requires collaboration with cross-functional teams, regulators, patients, caregivers, payers, and external partners across multiple therapeutic areas.

Manage and monitor clinical trial sites including qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, patient safety, query resolution, and contribute to study documentation and reports.

Conduct site selection, initiation, monitoring, and close-out visits across clinical trials. Ensure compliance with ICH-GCP, regulations, and SOPs; maintain CTMS and eTMF documentation; monitor patient safety, drug accountability, recruitment, retention, and data quality; resolve site issues; track training, budgets, and payments; and collaborate with clinical teams.

Conduct clinical trial monitoring for early-stage oncology studies, including site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and support clinical study documentation. Requires at least two years of Clinical Research Associate experience, oncology monitoring expertise, a scientific or healthcare degree, and willingness to travel up to 50% within the assigned region.