Compensation: CAD 120,000 - CAD 150,000 - yearly We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. We work on the frontline of medical science, changing lives, and bringing recent medicines to those who need them. We are looking for an experienced freelance Sr. Conduct and reportSIV, RMV,COVonsite monitoring visits Be responsible for site communication and management Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress Participate in feasibility research Support regulatory team in preparing documents for study submissions Prepare and particiapte on audits and inspections College/University degree in Life Sciences or an equivalent combination of education, training &

experience Experience in all types of monitoring visits in Phase II and/or III Experience in Oncology is a plus Full working proficiency in English and French. Proficiency in MS Office applications Ability to travel This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research. #

📌 Clinical Research Monitoring Specialist Senior (Toronto)
🏢 PSI CRO
📍 Toronto