Senior CRA

PSI CRO; Vancouver; On-site; CAD 65,000 - 85,000; Full time

Job summary

A leading Contract Research Organization in Canada is seeking a Clinical Research Associate to conduct monitoring visits and support clinical studies. The ideal candidate will have a degree in Life Sciences, independent monitoring experience, and be fully proficient in English and French. This role offers a dynamic team environment and the opportunity to grow within the clinical research field.

Qualifications

• Independent on-site monitoring experience.
• Experience in all types of monitoring visits in Phase II and/or III.
• Ability to travel as needed.

Responsibilities

• Conduct on-site monitoring visits and report findings.
• Perform CRF review and source document verification.
• Be responsible for site communication and management.

Skills

Fully fluent in English

Fully fluent in French

Planning and multitasking

Communication skills

Collaboration skills

Problem-solving skills

Education

College/University degree in Life Sciences

Tools

MS Office applications

Job description

Overview

PSI is a leading Contract Research Organization with 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 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.

Responsibilities

• Conduct on-site monitoring visits (SIV, RMV, COV) and report findings
• 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
• Prepare and participate in audits and inspections

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent on-site monitoring 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 is essential.
• 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

Additional Information

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