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.

Coordinates and conducts clinical trial procedures according to study protocols, including venipuncture, specimen processing, vital signs, ECGs, infusions, monitoring, testing, and injections. Collects accurate patient data, supports participant recruitment and enrollment, provides nursing care, and collaborates with study teams to maintain compliance, quality, and regulatory standards. The role is fully onsite, Monday through Friday, with no weekend or holiday work.

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.

Manage day-to-day clinical trial operations, including planning, timelines, budgets, protocols, stakeholder relationships, regulatory compliance, vendor selection, risk management, and clinical deliverables. Support cross-functional teams and develop team members while ensuring high-quality study outcomes. The role requires a relevant university degree, therapeutic-area expertise, clinical trial management experience, and approximately 25% travel.

Lead clinical data science initiatives supporting clinical trial analysis and strategic decision-making. Responsibilities include designing data science strategies, identifying analytical requirements, overseeing statistical models and tools, mentoring team members, and communicating insights to stakeholders. The role requires clinical research data analysis experience, statistical software expertise, data visualization skills, leadership, collaboration, and approximately 15% travel.

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and contribute to study documentation, protocols, and clinical study reports. Requires at least two years of CRA experience, scientific or healthcare education, strong organizational and communication skills, and approximately 60% travel.

Oversee clinical trial monitoring for sponsor-dedicated oncology studies, ensuring site adherence to protocols, regulations, and GCP standards. Conduct site visits, resolve performance issues, support data integrity, train site staff and CRAs, and collaborate with cross-functional stakeholders. Manage multiple sites and projects independently while maintaining strong relationships and driving compliance. The role requires approximately 60% travel.

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.

Conducts oncology clinical trial monitoring for assigned investigative sites, including site qualification, startup, initiation, monitoring, closeout, source document verification, query resolution, investigational product accountability, SAE reporting, regulatory compliance, and clinical data review. Communicates site status, resolves trial issues, maintains tracking systems and essential documents, and provides leadership or subject-matter expertise on complex studies and monitoring activities.

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%.

Monitor clinical trials including 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 contribute to study documentation and reports.

Monitor and manage clinical trial sites including qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; perform data review and query resolution; collaborate with investigators and site staff; contribute to study documentation and clinical study reports.

Lead clinical trial monitoring activities to ensure protocol and regulatory compliance, conduct site visits, resolve issues, support data integrity, train site staff and CRAs, collaborate cross-functionally, and maintain strong site relationships to drive successful trial execution.

As a Global Study Manager, you will lead projects, manage cross-functional teams, and ensure successful project execution while mentoring team members.