Jobs at ICON plc

Prepare and lead development of client-focused proposals, budgets, and client grids for Early Phase opportunities. Coordinate cross-functional input, chair kickoffs, support negotiations and bid defenses, and submit final proposals on time. Travel ~5%.

Leads end-to-end clinical data review and delivery activities across studies, ensuring quality, timeliness, budget adherence, and data fitness for analysis. Oversees analytic review, clinical system development input, risk management, planning, resourcing, and audit participation. Serves as the primary contact for internal and external stakeholders, manages multiple projects, and provides leadership, mentoring, and subject matter expertise. The role requires approximately 15% domestic or international travel.

Conducts bioanalytical LC-MS assays and prepares biological samples for pharmaceutical and chemical company studies. Responsibilities include operating laboratory equipment, analyzing and interpreting complex data, following study and validation plans, maintaining regulatory compliance, reviewing bioanalysis and method-validation results, preparing solutions, documenting work, and training junior analysts.

Manages country-level clinical trial operations, regulatory submissions, budgets, contracts, payments, vendors, site readiness, timelines, and compliance. Coordinates with clinical, finance, legal, regulatory, pharmacovigilance, vendors, sites, ethics committees, and regulatory authorities. Develops local-language materials, oversees study supplies and filings, manages risks, and supports process improvement, training, mentoring, and country-specific trial delivery.

Designs and implements clinical systems for research trials, including CRFs, edit checks, dynamic checks, database specifications, and post-production changes. Reviews requirements, conducts quality control, leads specification meetings, supports timelines and change management, and mentors junior team members. Requires clinical research systems experience, clinical data management expertise, familiarity with Medidata Rave or Veeva EDC, CRF design capability, strong communication skills, and a relevant bachelor’s degree.

Leads the design, development, review, and implementation of clinical systems for clinical trials. Designs CRFs, edit checks, dynamic checks, and database specifications; performs quality reviews; manages post-production database changes; supports timelines, change management, and study decision-making. Requires clinical research systems experience, CDMS expertise, protocol interpretation, and knowledge of platforms such as Medidata Rave or Veeva EDC. The role is remote in Canada with approximately 10% domestic or international travel.

Leads clinical data science workstreams for clinical trials, overseeing data management strategies, analysis, integration, governance, quality, regulatory compliance, and timely delivery. Collaborates with cross-functional stakeholders, provides strategic guidance, develops teams, and uses data analysis, statistical software, and visualization techniques to inform study decisions. Requires approximately 15% travel.

Supports global oncology clinical studies from start-up through close-out. Responsibilities include vendor procurement, contracting, budgets, documentation, risk tracking, stakeholder communications, CRO liaison, study registration, site and investigator contracting, ethics approvals, committee preparation, payments, system close-out, archiving, and final document management. The role requires clinical research industry experience, particularly in oncology, Phase IV, or real-world evidence studies, along with strong organization and stakeholder management skills.

Assess clinical trial data risks, monitor data quality and integrity, recommend mitigation strategies, collaborate on risk management plans, analyze and visualize findings, and support regulatory documentation and audits while communicating with English- and Mandarin-speaking stakeholders.

Manage investigator portals throughout clinical trials, including content, communications, surveys, forms, dashboards, user access, launches, and archiving. Partner with study teams, sites, vendors, and internal stakeholders to support engagement strategies, monitor activity, resolve issues, and improve the site experience. The role also facilitates meetings, supports training and documentation, and contributes to technology and process improvement initiatives.

Supports the preparation, processing, labeling, storage, tracking, documentation, and shipment of biological samples for Phase I clinical research studies. Prepares laboratory materials, maintains equipment and inventory, follows GCP, GLP, SOP, safety, and quality requirements, and collaborates with clinical and laboratory teams to ensure accurate, compliant sample handling.

Manage clinical trial operations from planning through delivery, ensuring timelines, budgets, quality standards, regulatory compliance, and ethical conduct. Collaborate with cross-functional teams, investigators, vendors, and stakeholders; oversee protocols and procedures, resolve trial-design and risk issues, and support clinical deliverables and team development. Travel of approximately 25% may be required.

Supports the configuration, testing, implementation, maintenance, and optimization of clinical trial systems, including EDC and CTMS. Assists with troubleshooting, user support, system upgrades, user acceptance testing, documentation, process development, and system performance monitoring. Collaborates with cross-functional clinical research teams and develops expertise in clinical technology and trial operations.

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 help prepare study documentation, protocols, and clinical study reports. The role is office-based in Shanghai and requires at least 60% international and domestic travel, including driving.

Manages clinical trial activities in China within ICON’s clinical research organization, supporting the development and delivery of new medicines and treatments. The posting provides limited role-specific responsibilities and qualifications, but emphasizes collaboration, accountability, regulatory-quality delivery, and patient-focused clinical research.

Coordinates site documentation, status tracking, metrics, logistics, and operational support for clinical research studies. Acts as a liaison for site staff, maintains compliance records, supports meetings and monitoring visits, identifies workflow improvements, and contributes to efficient study start-up and maintenance. The role also provides guidance to junior colleagues and collaborates with cross-functional teams.

Lead statistical programming for clinical trials, developing and validating SAS programs, collaborating with biostatisticians, performing quality control, preparing regulatory reports and publications, and improving programming processes. The role requires independent work, technical leadership, strong statistical knowledge, and effective communication in a clinical research environment.

Perform clinical trial monitoring activities including study setup, site monitoring, documentation maintenance, query resolution, stakeholder communication, and ensuring compliance with protocols, ICH-GCP, and regulatory requirements while supporting study cost efficiency.

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 support preparation and review of protocols and clinical study reports.

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. The role is home based in Hangzhou and requires approximately 60% travel.