Jobs at ICON plc

Lead site management and monitoring for Oncology clinical trials, performing on-site and remote visits, ensuring data integrity and subject safety, managing TMF/essential documents, driving site activation and engagement, monitoring KRIs, implementing CAPAs, supporting IRB/EC submissions and regulatory inspections, and mentoring/joining oversight activities.

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.

Lead and coordinate medical affairs projects and programmes, develop detailed plans, manage timelines/budgets/resources, lead cross-functional teams, monitor risks and progress, engage stakeholders, and prepare status reports while building team capability and resolving issues to ensure on-time, on-budget delivery.

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

Accountable for end-to-end country-level trial delivery for oncology and multi-therapeutic studies: vendor and vendor PO management, local milestones, resourcing, inspection readiness, cross-functional coordination with LTMs/LSMs/CTAs/SCMs, reporting to Functional Manager and Global Trial Leader, and supporting documentation, training, and ad hoc country-level issue resolution.

Lead Clinical Data Science project teams to plan, set up, maintain and close clinical data systems. Provide technical review, support sales/bid defense, oversee system integration and vendor interactions, manage timelines/budgets, perform CRF and UAT peer review, and act as primary contact for internal and external stakeholders.

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.