Jobs at ICON plc

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.

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.

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 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.

As a Clinical Research Associate, you will monitor Oncology studies, coordinate activities, ensure compliance, and maintain strong relationships with stakeholders to ensure patient safety and efficient study operations.

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.

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 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 Global Study Manager, you will oversee clinical budgets, develop monitoring plans, manage study start-ups, drive enrollment, and foster relationships with stakeholders.

As Global Study Lead, you will manage clinical trial aspects, focusing on budget oversight, study monitoring, enrollment, and stakeholder relations.

The Global Study Manager will lead project management activities, develop plans, guide teams, and collaborate with stakeholders to ensure project success in the pharmaceutical or biotech industry.

As a Manager of Clinical Operations, you will oversee clinical trials, ensuring compliance with regulations, optimizing processes, and mentoring junior staff while maintaining stakeholder communications.

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.