Jobs at ICON plc

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.

Serve as primary contact between investigational sites and sponsor; perform site selection, initiation, routine monitoring, and close-out; ensure ICH‑GCP and Health Canada compliance; maintain CTMS/eTMF documentation; monitor safety reporting (AE/SAE/PQC); support recruitment, drug accountability, data query resolution, site budgets/payments, and escalate risks to the clinical team.

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.

As a Clinical Research Associate, you will conduct site visits, ensure data integrity and patient safety, and collaborate on study documentation.

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.