Jobs at Centricity Research

Coordinates patient recruitment and retention for clinical trials, screens candidates against study protocols, conducts informed consent and screening visits, collects vital signs and medical histories, maintains recruitment databases and trial documentation, resolves data queries, tracks enrollment metrics, and supports outreach events. The role works closely with site management, research operations, investigators, and regional research sites.

Supports digital marketing and patient recruitment campaigns by launching ads, monitoring KPIs, analyzing performance, updating study materials, coordinating sponsor revisions, and tracking deliverables. The role collaborates with internal teams, sponsors, and external partners while maintaining accurate campaign information and compliance-aligned content across multiple platforms.

Configures and maintains study-specific electronic source documents, CTMS visit templates, financial workflows, billing items, and study schedules. Reviews clinical trial agreements and budgets, supports study teams and site users, troubleshoots CTMS issues, and ensures configurations align with protocols, company standards, and regulatory requirements throughout the study lifecycle.

Supports Phase I-IV clinical research studies through participant recruitment and screening, informed consent, clinical assessments, phlebotomy, sample processing, data entry, adverse-event reporting, investigational product accountability, and study documentation. Maintains compliance with protocols, GCP, SOPs, and regulations while assisting with monitoring visits, audits, scheduling, laboratory preparation, and participant check-in. This fully onsite role works closely with investigators, coordinators, and site staff Monday through Friday.

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.

Leads accounting and finance operations across US and Canadian entities, overseeing reporting, treasury, audits, tax compliance, internal controls, finance systems, acquisitions, refinancing, and financial integration. The VP develops the finance team, drives process automation and technology adoption, prepares executive and board reporting, and advises leadership and private equity stakeholders on financial strategy and organizational growth.

Serve as site Principal Investigator overseeing endocrine clinical trials, ensuring patient safety, regulatory compliance, data integrity, informed consent, and adverse event reporting. Provide direct clinical care to clinic and research patients, supervise research staff, maintain audit-ready documentation, and liaise with sponsors, IRBs, and company teams to run trials ethically and efficiently.