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Provide technical expertise for clinical trials, support programming activities related to clinical study data analysis and reporting. Specialize in therapeutic areas and ensure regulatory compliance.

Responsible for planning and delivering EUCTD/R reporting, coordinating with various teams, managing documents, and engaging with vendors for Clinical Trial Applications.

The TMF Records Specialist manages Trial Master File operations, including setup, maintenance, and closeout, ensuring compliance with trial protocols, regulations, and documentation standards.

The Financial Analyst I role involves financial analysis, budgeting, forecasting, and reporting for project financials, contributing to improved revenue and cash flow management.

The Project Management Assistant supports project managers with administrative tasks including document preparation, communication facilitation, and project organization, aimed at improving clinical trial processes.

The Meetings Specialist leads project deliverables in Meeting Services, manages pharmaceutical events, and ensures high-quality execution while meeting client expectations and budget constraints.

The Statistical Programmer II assists in project management, statistical programming, and training while ensuring regulatory compliance and quality standards.

As a Clinical Research Associate, you will oversee site selection, train site staff, and ensure study documentation is managed for clinical trials, focusing on oncology.

The Site Contract Leader oversees site contracting for clinical trials, managing budgets, risks, developing project documents, and ensuring effective stakeholder communication.

The Document Quality Reviewer II ensures high-quality clinical documents through thorough reviews for grammar, accuracy, and adherence to style guides, while supporting training and process improvement initiatives.