Jobs at ICON plc

Lead and conduct clinical trial monitoring to ensure protocol and GCP compliance. Perform site visits, resolve issues, support data quality, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to ensure timely trial execution. Role is sponsor-dedicated and based in the GTA with ~60% travel.

Manage site start-up and activation tasks for assigned clinical trial sites, including collection and review of essential documents, eTMF accuracy, ICD/ICF review, tracking actions and timelines, escalating delays, and collaborating with CROs and internal teams to improve site activation metrics and resolve issues.

Lead design, deployment and management of eCOA/ePRO systems for decentralized trials. Serve as sponsor SME and project manager, define requirements, oversee UAT, vendor selection and oversight, resolve system issues, integrate eCOA data with CTMS and data warehouses, ensure documentation and audit readiness, provide training, and coordinate cross-functional delivery within timelines and budgets.

The Senior Clinical Research Associate will monitor clinical studies, ensuring compliance with protocols, SOPs, ICH-GCP, and regulatory requirements. They will also support the development of drugs and devices that improve quality of life.

Manage and analyze clinical trial contracts and vendor agreements, negotiate terms, assess contract risk and compliance, maintain contract records in management systems, and advise internal teams on contract interpretation and dispute resolution.

Manage implementation and delivery of IRT solutions for clinical trials. Lead project planning, timelines, budgets, stakeholder communication, cross-functional collaboration, and compliance while driving quality and innovation in IRT technologies.

The Country Study Operations Manager oversees clinical trial operations across countries, ensuring compliance and timely execution, while managing budgets and resources effectively.

As a Clinical Trial Transparency Anonymization Specialist, you will manage the anonymization of clinical trial documents and datasets for public disclosure, collaborating with various teams to ensure compliance with regulatory requirements.

Lead development and analysis of pricing strategies and investigator payments for clinical trials. Collaborate with clinical operations and finance, build pricing models, conduct benchmarking and financial analysis, prepare pricing reports, ensure regulatory and policy compliance, and recommend cost optimizations.

The Senior Study Manager oversees clinical trial operations, managing teams, vendor interactions, budgets, timelines, and ensuring compliance and quality control throughout the study process.

The Senior Study Manager will oversee clinical trial activities, manage operational deliverables, vendor interactions, and ensure compliance with protocols and budgets while leading the Clinical Trial Team.

The Informed Consent Writer is responsible for preparing health literate informed consent documents for clinical trials across multiple therapeutic areas, ensuring clarity and compliance with regulations.

As a Study Start Up Associate II, you will facilitate clinical trial initiation, prepare regulatory documents, and collaborate with stakeholders for approvals.

The Manager oversees contracts management, negotiating agreements, ensuring compliance, and supporting project teams with contract-related issues.

Edit and proofread clinical and regulatory documents, ensure compliance with guidelines, mentor junior staff, fact-check data, implement SOPs, and collaborate with writers to improve scientific communications.

Coordinate site activations and maintenance across studies; collect and review Critical Document Packages (CDPs); forecast activation dates; liaise with sites, sponsors, and internal stakeholders; ensure regulatory/IRB submissions and TMF quality; manage translations, CTAs/budgets support, escalate issues, and mentor team members while driving process improvements and KPI achievement.

The Senior Clinical Research Associate will monitor clinical studies compliance and conduct, ensuring adherence to protocols and regulations. Responsibilities include overseeing trials at sites and preparing reports.

The Senior Clinical Research Associate monitors clinical studies, ensuring they comply with protocols and regulations while documenting progress both on-site and remotely.

Lead Clinical Data Science project teams to plan, set up, maintain and close clinical data systems. Provide technical review, support sales/bid defense, oversee system integration and vendor interactions, manage timelines/budgets, perform CRF and UAT peer review, and act as primary contact for internal and external stakeholders.

The Study Start Up CRA is responsible for site selection, start up activities, ensuring compliance with relevant regulations, and collaborating with various stakeholders to meet study timelines.