CRA II: Onsite Monitoring & Study Startups

Psi CRO; Quebec; On-site; CAD 98,000 - 120,000; Full time

Job summary

PSI is seeking a Clinical Research Associate II to join our team and support clinical studies across diverse therapeutic indications. You will conduct onsite monitoring visits and contribute to study startup, CRF review, and sponsor communications.

The ideal candidate has on-site monitoring experience in North America, is fluent in English and French, and can travel as needed. This role offers growth within a leading CRO and opportunities to broaden therapeutic area expertise.

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience.
• Independent on-site monitoring experience in North America.
• Experience in all types of monitoring visits in Phase II and/or III.
• Full working proficiency in English and French.
• Proficiency in MS Office applications.
• Ability to travel.
• Valid driver’s license.

Responsibilities

• Conduct and report all types of onsite monitoring visits.
• Participate in study startup activities when applicable.
• Perform CRF review, source document verification and query resolution.
• 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.

Skills

On-site monitoring

Phase II/III monitoring

English and French fluency

Travel readiness

Education

Life Sciences degree or equivalent

Tools

MS Office

Job description

PSI is seeking a Clinical Research Associate II to join our team and support clinical studies across diverse therapeutic indications. You will conduct onsite monitoring visits and contribute to study startup, CRF review, and sponsor communications.

The ideal candidate has on-site monitoring experience in North America, is fluent in English and French, and can travel as needed. This role offers growth within a leading CRO and opportunities to broaden therapeutic area expertise.