Jobs at ICON plc

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 Study Start Up Associate facilitates clinical trial initiation by preparing regulatory documents, coordinating approvals, and supporting study teams.

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

Support Global Study Directors and Managers by managing the electronic trial master file, coordinating study documents, and ensuring compliance with regulatory standards.

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 Global Studies Associate supports Global Study Directors and Managers by managing eTMF setups, regulatory document collections, and administrative tasks throughout clinical studies.

Assist in the coordination and administration of clinical trials, ensure compliance, maintain documentation, and support study material preparation.

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.

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

Lead and oversee Phase I-II clinical trials as the Senior Principal Biostatistician, providing statistical input and mentoring junior statisticians.

As a Contract Analyst II, you'll manage contract deliverables, review legal documents, negotiate terms, and support internal teams.

As a Contract Analyst II, you will manage contracts for clinical trials, ensuring compliance and efficiency through analysis, negotiation, and collaboration with teams.

The Contract Analyst II will manage contract deliverables, review agreements, negotiate terms, collaborate on risks, and support teams on compliance.

The Start Up Project Manager oversees global study start up activities, ensuring site activations and project timelines meet targets across clinical trials.

As a Clinical Operations Study Lead at ICON, you'll manage projects, lead teams, develop project plans, and mentor staff to ensure successful project execution in clinical settings.

Oversee and monitor clinical trial sites to ensure GCP and protocol compliance, conduct site visits, resolve issues, ensure data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to support trial execution.

The Senior Issue Lead manages Major Quality Event investigations, coordinates audits, ensures compliance with GCP standards, and trains Issue Leads. This role involves root cause analysis, process improvement, and leading quality assessments.

The Third Party Quality Lead manages third-party quality risks in clinical operations, ensures GCP compliance, and oversees vendor performance and quality systems.