Teams at Centricity Research

Supports Phase I-IV clinical research studies across multiple Toronto-area sites. Responsibilities include participant recruitment and consent, phlebotomy, vitals and ECGs, follow-up visits, sample processing, data entry, chart and query reviews, adverse-event reporting, investigational product accountability, documentation, and audit preparation. Regular travel between sites is required.

Coordinate Phase I-IV clinical trials at a Toronto site: conduct participant visits and phlebotomy, ensure participant safety and protocol compliance, manage recruitment/screening/consent, maintain study documentation, support monitoring/audits, and assist site start-up and site operations.

Supports budgeting, forecasting, variance analysis, cash-flow management, financial modeling, and recurring reporting across corporate and site-level cost centers. Builds dashboards and KPI tracking, maintains shared financial models, partners with operational and clinical leaders, and contributes to integrated P&L, balance sheet, and cash-flow modeling. The role also helps automate reporting and establish FP&A processes and best practices.