Jobs at ICON plc

Conduct site selection, initiation, monitoring, and close-out visits for clinical trials across therapeutic areas. Ensure ICH-GCP and regulatory compliance, maintain CTMS and eTMF documentation, monitor patient safety and drug accountability, support recruitment and data quality, resolve issues, track budgets, and collaborate with clinical teams. The role requires 60%–75% travel for on-site monitoring visits.

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 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.

Conduct site selection, initiation, monitoring, and close-out visits for clinical studies across therapeutic areas. Ensure ICH-GCP, regulatory, and SOP compliance; maintain CTMS and eTMF documentation; monitor patient safety, recruitment, data quality, drug accountability, training, budgets, and payments. Serve as the liaison between investigational sites and sponsors, escalate risks, and collaborate with clinical team members. Requires 60%–75% regional travel across the Midwest.

Conduct site selection, initiation, monitoring, and close-out visits for clinical trials. Ensure compliance with ICH-GCP and regulations, 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 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.

Leads full-scope clinical project and program management for oncology and hematology studies, including radiopharmaceutical and radioligand programs. Develops project plans, manages cross-functional teams and stakeholders, oversees documentation and reporting, mentors team members, and ensures quality delivery against project objectives. Requires extensive CRO project management experience, oncology expertise, strong leadership and communication skills, and willingness to travel approximately 25%.

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.

Lead and coordinate oncology clinical trials including start-up, recruitment, protocol execution, training, monitoring, adverse event reporting, sponsor relations, internal quality review, and cross-site travel within the Accellacare network.

Lead and perform clinical trial monitoring and site management for oncology Phase II/III studies, ensuring ICH GCP and local regulatory compliance, site start-up, source data verification, SAE reporting, IP accountability, issue escalation, and documentation. Acts with limited oversight and may lead complex studies or serve as a subject-matter expert.

The Clinical Research Associate will monitor sites for compliance, manage documentation, ensure patient safety, facilitate training, and oversee drug accountability in oncology trials.

Conduct site management and monitoring for oncology clinical trials, including qualification, initiation, interim, and close-out visits. Ensure data integrity, subject safety, inspection readiness, regulatory compliance, and essential document reconciliation. Manage site relationships, feasibility, activation, IRB/EC submissions, risk indicators, and CAPA plans. Train site staff on protocols, GCP, SOPs, and regulations, while supporting inspections and mentoring junior CRAs. The role requires solid tumor oncology trial expertise and travel up to 50%.

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.

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.

Leads clinical data science project teams supporting the setup, maintenance, integration, quality control, and closure of clinical trial systems. The role involves client and vendor coordination, technical documentation review, CRF quality review, timeline and budget tracking, system integration oversight, sales support, and internal user acceptance testing. Candidates need clinical data management experience, relational database knowledge, data flow diagramming skills, project management capabilities, protocol interpretation expertise, strong communication skills, and a bachelor's degree.

Coordinate and execute sponsor contracts and change orders for early-phase clinical research projects. Responsibilities include reviewing contractual terms, budgets, payment schedules, and project documents; collaborating with legal, sales, finance, operations, and project teams; analyzing financial implications; maintaining Salesforce records and contract files; supporting client negotiations; and managing multiple deadlines while ensuring accurate quality-control submissions.

Oversee clinical trial sites and ensure protocol, regulatory, and GCP compliance. Conduct site visits, assess performance, resolve issues, support site staff, and maintain data integrity and participant safety. Collaborate with cross-functional teams on data collection and reporting, train site personnel and CRAs, and manage relationships with stakeholders. The role requires extensive CRA experience, advanced relevant education, strong monitoring and organizational skills, and travel of at least 60%.