Conduct clinical monitoring at PSI across therapeutic indications, applying source verification and query resolution expertise. Travel throughout North America for onsite visits.
As a Clinical Research Associate II, you will support clinical studies while maintaining PSI's quality standards. The work includes monitoring visits, site management, study startup, and regulatory support. You will communicate with project teams, vendors, and support services throughout study delivery.
Key Responsibilities:
- Conduct and report all types of onsite monitoring visits
- Perform CRF review and source document verification
- Resolve queries and manage site communications
- Communicate study progress with internal project teams
- Support regulatory documents and feasibility research
Requirements:
- Life Sciences degree or equivalent education, training, and experience
- Independent North American onsite monitoring experience
- Phase II and/or III monitoring visit experience
- Full working proficiency in English and French
- MS Office proficiency and ability to travel
Apply clinical monitoring, site management, and bilingual communication skills as a Clinical Research Associate II at PSI.
Clinical Research Associate II Monitoring in Toronto employer: PSI CRO
At PSI, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. As a Clinical Project Management Lead, you will benefit from our commitment to employee development, competitive compensation, and the opportunity to make a meaningful impact in clinical research across North America. Join us in a dynamic environment where your leadership will drive success and contribute to advancements in healthcare.
