Senior Clinical Research Associate

PSI CRO; Toronto; On-site; CAD 120,000 - 150,000; Full time

Job summary

PSI CRO in Canada seeks an experienced freelance Sr. CRA to support our clinical trials. You will conduct and report SIV, RMV, COV onsite monitoring visits and perform CRF review, source document verification and query resolution.

Ideal candidates have Phase II/III monitoring experience, Oncology exposure is a plus, and you must be fluent in English and French. Travel and valid driver's license are required.

Qualifications

• College/University degree in Life Sciences or equivalent.
• Experience in all types of monitoring visits in Phase II and/or III.
• Experience in Oncology is a plus.
• Proficiency in English and French.
• Proficiency with MS Office applications.

Responsibilities

• Conduct and reportSIV, RMV,COVonsite monitoring visits
• 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 particiapte on audits and inspections

Skills

Communication skills

Multitasking

Team collaboration

Problem solving

Travel flexibility

Education

College/University degree in Life Sciences

Tools

MS Office

Job description

• Compensation: CAD 120,000 - CAD 150,000 - yearly

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:

• Conduct and reportSIV, RMV,COVonsite monitoring visits
• 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 particiapte on audits and inspections

Qualifications

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

Additional Information

For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.

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