Jobs at ICON plc

Facilitates clinical trial site activation by preparing regulatory and ethics submissions, coordinating approvals, maintaining submission records, supporting study document development, and contributing to start-up meetings. The role requires collaboration with internal and external stakeholders, strong organization, attention to detail, and the ability to manage multiple tasks independently in a fast-paced environment.

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 the development, validation, and maintenance of clinical data programming solutions for EDC/CDMS systems, vendor data, analytics, reports, integrations, and data transfers. Provide technical leadership across studies, serve as a programming subject matter expert, mentor programmers, support study teams, and drive automation and process improvements. Collaborate with data managers, biostatisticians, and project managers to ensure high-quality clinical trial data management solutions.

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.

Designs and implements clinical systems for research trials, including CRFs, edit checks, dynamic checks, database specifications, and post-production changes. Reviews requirements, conducts quality control, leads specification meetings, supports timelines and change management, and mentors junior team members. Requires clinical research systems experience, clinical data management expertise, familiarity with Medidata Rave or Veeva EDC, CRF design capability, strong communication skills, and a relevant bachelor’s degree.

Leads the design, development, review, and implementation of clinical systems for clinical trials. Designs CRFs, edit checks, dynamic checks, and database specifications; performs quality reviews; manages post-production database changes; supports timelines, change management, and study decision-making. Requires clinical research systems experience, CDMS expertise, protocol interpretation, and knowledge of platforms such as Medidata Rave or Veeva EDC. The role is remote in Canada with approximately 10% domestic or international travel.

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.

As a Global Study Manager, you will lead projects, manage cross-functional teams, and ensure successful project execution while mentoring team members.