Site Jobs in Fort Frances, ON
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Site • fort frances on
- Promoted
CRA I / II / III- FSP large pharma
ICON Strategic SolutionsOntario, Canada, CanadaMaintenance Site Supervisor
York UniversityOntario, CanadaSenior Site Services Planner (contract)
Agnico EagleOntario-Cochrane-Detour LakeHVAC / Refrigeration Mechanic
Tundra Site ServicesON., CA- New!
professional land surveyor
Surveyors On Site Inc.ON, CA- Promoted
Underground Red Seal Mine Electrician ($60 to 65 per hour)
WORKFORCE - Staffing SolutionsAlgoma, ON, Canada- Promoted
Neurologist
Headlands Research, Inc.Golden Horseshoe, ON, Canada- Promoted
Project Manager - Civil
EBC Inc.White's Falls, ON, caSite Supervisor
Royal Architectural Institute of CanadaOntario- New!
Site Reliability Engineer
SGSON, CanadaHSE - Safety Advisor - Construction Site
Dokainish & CompanyOntario, ON, CARemote Site Technician - Mining
Toromont CatON, CASite Activation Partner - FSP
ParexelRemote, Ontario, CanadaSite Manager – Niagara Falls / Chippawa, ON
gcpCanadá , OntarioSite Supervisor – Civils and Infrastructure / Ontario, Canada
Shackleton Duke GroupOntario, CanadaOntario Nurse Practitioner (NP) | Clinic | Virtual & On-Site Options
HealthOPMOntario, Canada- Promoted
Digital Marketing Specialist (on-site)
ScotlynnNorfolk County, ON, CanadaHead of Operations & Site Manager - Ontario, CA
ZEISS GroupOntario, CA- Promoted
Site Supervisor
The Burke Group : Human Resources SpecialistsNiagara, ON, CanadaCloud Site Reliability Engineer
Magnet ForensicsOntarioCRA I / II / III- FSP large pharma
ICON Strategic SolutionsOntario, Canada, Canada- Full-time
Key Responsibilities
Conduct on-site and remote monitoring visits per the Monitoring Plan.
Perform Source Data Review (SDR), Source Data Verification (SDV), and Case Report Form (CRF) review.
Conduct Site Quality Risk Assessments and adjust monitoring intensity as needed.
Train and support Investigators and site staff on study procedures and Risk-Based Quality Management (RbQM) principles.
Ensure ICH-GCP compliance and site inspection readiness at all times.
Manage study drug supplies and accountability, including preparation for destruction if applicable.
Escalate quality issues, protocol deviations, and compliance concerns per AZ procedures.
Submit and track essential regulatory documents for study start-up and duration.
Provide timely monitoring reports and site performance updates.