Jobs at ICON plc

Manage day-to-day clinical trial operations, including planning, timelines, budgets, protocols, stakeholder relationships, regulatory compliance, vendor selection, risk management, and clinical deliverables. Support cross-functional teams and develop team members while ensuring high-quality study outcomes. The role requires a relevant university degree, therapeutic-area expertise, clinical trial management experience, and approximately 25% travel.

Supports the coordination and administration of clinical trials, including maintaining study files, preparing trial materials, managing regulatory documentation, coordinating cross-functional communication, and tracking clinical trial milestones and metrics while ensuring protocol and regulatory compliance.

Supports the coordination and administration of clinical trials, including maintaining study files, preparing regulatory and study materials, facilitating cross-functional communication, and tracking trial metrics and milestones. Ensures compliance with protocols, regulations, and guidelines while contributing to high-quality clinical research delivery.

Supports the coordination and administration of clinical trials, including maintaining study files, essential documents, and regulatory submissions. Prepares study materials, collaborates with cross-functional teams, and tracks clinical trial metrics and milestones while ensuring protocol and regulatory compliance.

Supports the coordination and administration of clinical trials, including maintaining study files, regulatory documentation, and essential records. Prepares trial materials, collaborates with cross-functional teams, and tracks clinical trial metrics and milestones. Ensures compliance with protocols, regulations, and guidelines while contributing to high-quality trial execution. The role is hybrid, requiring attendance at the Mississauga office three days per week.

Supports the coordination and administration of clinical trials, maintaining essential documentation and regulatory submissions, preparing study materials, collaborating with cross-functional teams, and tracking trial metrics and milestones. The role requires clinical research experience, knowledge of trial regulations, strong organization and communication skills, and attendance at the Mississauga office three days per week.

Supports clinical trial coordination and administration, maintains essential study and regulatory documentation, prepares trial materials, collaborates with cross-functional teams, and tracks clinical trial metrics and milestones. The role requires clinical research experience, regulatory knowledge, strong organization and communication skills, and attendance at the Mississauga office three days per week.

Supports clinical trial coordination, administration, documentation, regulatory submissions, study-material preparation, cross-functional communication, and tracking of trial metrics and milestones. Ensures compliance with protocols and regulatory requirements while maintaining organized study files and essential documents. The role requires clinical research experience, strong organizational and communication skills, attention to detail, and hybrid attendance at the Mississauga office three days per week.

Supports clinical trial coordination and administration, maintains essential study and regulatory documentation, prepares trial materials, collaborates with cross-functional teams, and tracks clinical milestones and metrics. The role requires clinical research experience, knowledge of trial regulations and processes, strong organization and communication skills, and in-office work in Mississauga three days per week.

Supports clinical trial coordination, administration, documentation, regulatory submissions, study-material preparation, cross-functional communication, and tracking of trial metrics and milestones. Ensures activities comply with protocols and regulatory requirements while maintaining organized study files. The role requires a scientific or healthcare-related bachelor’s degree, at least two years of clinical trial support experience, regulatory documentation experience, strong organizational and communication skills, and hybrid attendance in Mississauga three days weekly.

Supports the coordination and administration of clinical trials, maintaining study documentation, regulatory submissions, and trial materials. Collaborates with cross-functional teams, tracks clinical trial metrics and milestones, and ensures compliance with protocols and regulatory requirements. The role requires strong organization, communication, attention to detail, and the ability to work from the Mississauga office three days per week.

Supports clinical trial coordination, administration, documentation, regulatory submissions, study-material preparation, cross-functional communication, and tracking of trial metrics and milestones. The role requires maintaining compliance with protocols and regulations while organizing essential clinical research files and supporting smooth trial execution. This is a hybrid position requiring three days per week in the Mississauga office.

Supports the coordination and administration of clinical trials, including maintaining study and regulatory documentation, preparing trial materials, tracking milestones, and facilitating cross-functional communication. Ensures compliance with protocols and applicable regulations while contributing to accurate reporting and smooth trial execution. The role requires a scientific or healthcare-related bachelor's degree, at least two years of clinical trial support experience, strong organizational skills, and hybrid attendance in Mississauga three days per week.

Supports clinical trial site activation by preparing regulatory and ethics submissions, coordinating approvals, maintaining submission records, assisting with study documents, and contributing to start-up meetings. The role requires cross-functional collaboration, strong organization, attention to detail, and approximately 5% travel.

Supports clinical trial coordination and administration, maintains essential study and regulatory documentation, prepares trial materials, coordinates cross-functional communication, and tracks clinical milestones and metrics. Ensures work complies with study protocols, regulations, and guidelines while contributing to high-quality clinical research in a hybrid environment.

Facilitates clinical trial site initiation and activation by preparing regulatory and ethics submissions, coordinating approvals, maintaining submission records, supporting study document development, and advising on regulatory requirements and timelines. Collaborates with internal and external stakeholders while managing multiple tasks in a fast-paced environment. The role requires a life sciences degree, strong organization and communication skills, and approximately 5% travel.

Oversee and coordinate oncology clinical trials, ensuring protocol adherence, regulatory compliance, data integrity, quality, and timely execution. Manage site activities, collaborate with cross-functional teams and investigators, support clinical staff, monitor trial progress, identify risks, and implement mitigation strategies. The role requires independent work, strong organization, and effective stakeholder communication.

Lead and manage oncology clinical trials or a portfolio, serving as primary client liaison. Direct cross-functional teams and vendors, ensure contractual deliverables, timelines, budgets and risk mitigation. Prepare project financials and projections, participate in bid defense, and provide performance feedback to improve team delivery.

Oversee clinical trial monitoring for respiratory and cardiovascular studies, ensuring protocol, regulatory, and GCP compliance. Conduct site visits, assess performance, resolve issues, support data integrity, collaborate with cross-functional teams, train site staff and CRAs, and maintain stakeholder relationships. The role requires independent management of multiple sites and projects, strong clinical monitoring expertise, and approximately 60% travel.

Develops, validates, and maintains clinical data programming solutions for CDMS and clinical trials, including eCRFs, edit checks, data validation outputs, reports, extracts, transfers, and vendor data programs. Collaborates with cross-functional clinical data teams, supports study setup and maintenance, mentors junior programmers, creates training materials, and improves technical systems and processes.