The Analytical Monitor performs data analysis and risk management for clinical trials, collaborating with teams to ensure patient safety and compliance.

The RBQM Lead will implement and manage risk-focused quality oversight across clinical studies, collaborating globally with stakeholders to ensure effective risk management throughout the clinical trial lifecycle.

The Lead Clinical Data Science Programmer designs and develops clinical data solutions, ensuring efficient handling and analysis of trial data while collaborating with teams to drive insights for innovative therapies.

Prepare and maintain budgets, forecasts and P&L for business units; analyze monthly/quarterly results and KPIs; produce reporting packages and management presentations; support revenue pre-close, cost analysis, headcount management, and ad-hoc financial/business case analysis while partnering with project management.

As a Junior Statistician, you'll design statistical plans, conduct analyses on research data, and communicate findings. You will collaborate on reporting and ensure data integrity.

As a Junior Statistical Programmer at ICON plc, you will design and analyze clinical trials, develop programs for data analysis, and assist with regulatory submissions.

The role involves developing and validating statistical programs for clinical trials, collaborating with teams on analysis, and mentoring junior programmers.

Develop and validate R programs for statistical analysis of clinical trial data. Collaborate with biostatisticians, perform QC on outputs, prepare statistical reports for regulatory submissions, and support process improvements. PK and NONMEM expertise required.

Manage and process investigator payments, review invoices for accuracy and compliance, resolve payment queries with clinical and finance teams, maintain financial records for audits, and communicate payment procedures to investigators.

Support site activation by coordinating vendor access (eCRF, IVRS), managing CDP/submission documentation, maintaining study trackers, ensuring TMF completeness, applying ICH-GCP and SOPs, and collaborating with site partners and CRAs to enable timely study activation.

The Senior Financial Accountant leads a team to provide financial insights, manage project finances, prepare reports, and ensure the accuracy of financial data to support business objectives.

The Informed Consent Specialist will develop and review ICFs, ensure compliance with regulations, collaborate with stakeholders, and manage timelines. The role includes mentorship and maintaining documentation accuracy.

Manage negotiation, execution, and ongoing administration of clinical trial agreements and site budgets. Support site start-up, regulatory compliance, contract filing, risk escalation, and process improvements while collaborating with cross-functional teams and mentoring junior staff.

Lead cross-functional teams to plan, execute, and deliver pharmaceutical/biotech projects on time, within budget, and to quality standards. Manage scope, resources, risks, and stakeholder communications; develop project documentation and reports; mentor team members and integrate best practices to drive continuous improvement.

Lead the design, development, and validation of data science programming solutions for clinical trials, ensuring data accuracy and quality.

Lead implementation, optimization, and maintenance of clinical systems; collaborate with cross-functional teams to define requirements; monitor performance; provide training and stakeholder support to ensure data integrity and regulatory compliance.

Develop and validate statistical programming code for clinical trial data analysis and reporting, ensuring data integrity and compliance with standards.