Jobs at Centricity Research

Provide high-level administrative and operational support to executive and senior leadership: manage complex calendars and inboxes, coordinate meetings, travel, and board materials, maintain confidential records, publish internal communications via SharePoint, and partner with HR on employee engagement and events. Improve processes using Microsoft 365 and AI tools.

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.

Lead recruitment and screening for clinical trials: identify eligible patients, conduct outreach, obtain informed consent, perform screening tasks and vital signs, maintain CTMS/recordkeeping, support enrollment and community outreach, and provide recruitment metrics.

Support execution of Phase I-IV clinical trials: recruit and consent participants, perform phlebotomy and delegated clinical procedures, collect/process samples, maintain source documents/CRFs/CTMS, manage investigational product accountability, and prepare for monitoring visits and audits to ensure compliance and participant safety.

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.

Lead recruitment and screening for clinical trials: identify eligible participants, conduct outreach and inbound/outbound screening, obtain informed consent, collect vitals and source data, maintain recruitment and trial tracking systems, support site enrollment initiatives, attend community outreach events, and collaborate with central operations and investigators to optimize enrollment.

Support clinical trials from start to finish across two Quebec sites. Recruit and consent participants, perform autonomous blood draws, vitals, ECGs, POCT, collect/process/ship samples, maintain source documents/CRFs and CTMS, report adverse events, prepare for monitoring and audits, manage investigational product documentation, and collaborate with site teams to ensure GCP and protocol compliance.

Support execution of clinical trials by recruiting and screening participants, conducting visits and assessments (vitals, ECGs, phlebotomy), collecting and shipping samples, maintaining CRFs/CTMS/ISF, ensuring protocol/GCP compliance, and assisting with monitoring, audits, scheduling, and site administration.

Partner with People Operations to support employees across Canada and the U.S. Manage onboarding, offboarding, HRIS and benefits administration, employee relations, leave and compliance. Prepare workforce reports, drive process improvements using HR technology and AI, support audits and strategic projects, and provide backup recruitment support while building cross-functional relationships to deliver excellent employee experiences.

Coordinate Phase I-IV clinical studies at Centricity Research Vaughan, conducting participant visits and phlebotomy, ensuring protocol and regulatory compliance, performing clinical procedures (vitals, ECGs, sample handling), supporting recruitment, consent, documentation, QC, monitoring visits, audits, and site start-up activities while collaborating with investigators and supporting nearby Toronto sites as needed.

Coordinate and conduct study visits per protocol and GCP, ensure participant safety, perform phlebotomy and clinical procedures, recruit/screen/enroll participants, obtain informed consent, complete source documentation and EDC entry, support monitoring/audits, and maintain regulatory and site readiness.