Clinical Research Associate II

PSI CRO; Canada; On-site; CAD 65,000 - 95,000; Full time

Job summary

PSI CRO in Canada is seeking a Clinical Research Associate II to conduct onsite monitoring visits across multiple studies, ensuring high quality and regulatory compliance. You will support study startup, perform CRF review, source data verification, and query resolution, and maintain site communications.

Fluency in English and French, MS Office proficiency, and ability to travel are required. Join PSI CRO to broaden therapeutic experience and contribute to timely study submissions while working

Qualifications

• College/University degree in Life Sciences or 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 plan, multitask and work in a dynamic team environment.
• Communication, collaboration, and problem-solving skills.
• Ability to travel.
• Valid driver’s license.

Responsibilities

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup (if 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

English/French proficiency

Multitasking

Communication

Education

Life Sciences degree

Tools

MS Office

Job description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

As a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup (if 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

• 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 plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel
• Valid driver’s license

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.