Jobs at ICON plc

Lead coordination and oversight of clinical trial activities to ensure protocol adherence, regulatory compliance, site management, data integrity, risk identification, and cross-functional collaboration to support study execution and continuous improvement.

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 Informed Consent Writer prepares informed consent documents for clinical trials, ensuring clarity and compliance with regulatory guidelines, while collaborating with protocol authors.

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

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.

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.

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.

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 clinical trial monitoring activities to ensure protocol and regulatory compliance. Conduct site visits, resolve issues, support site staff, collaborate with cross-functional teams, train other CRAs, maintain data integrity, and manage multiple sites while fostering stakeholder relationships.

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.

The Informed Consent Writer prepares clinical trial informed consent documents, ensuring comprehension and compliance with health literacy standards through collaboration with protocol authors.

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

Lead regional clinical operations projects: develop and execute project plans, manage cross-functional teams, mentor staff, define scope with stakeholders, produce project documentation and reports, integrate industry best practices, and support organizational growth. Travel approximately 25%.

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.

As a Clinical Research Associate, you will conduct site visits, ensure data integrity and patient safety, and collaborate on study documentation.

The Feasibility Principal Analyst leads feasibility activities for clinical studies, analyzes data for enrollment strategies, and mentors junior team members.