Senior Clinical Research Associate

Psi CRO; Toronto; On-site; CAD 120,000 - 150,000; Part time

Job summary

Psi CRO in Canada is seeking an experienced freelance Senior CRA to support onsite monitoring across Phase II/III studies. You will conduct SIV, RMV, COV visits and oversee source data verification, query resolution, and site communications.

The ideal candidate has a Life Sciences degree, extensive monitoring experience, oncology exposure is a plus, excellent English, and the ability to travel with a valid driver's license. MS Office proficiency is required.

Qualifications

• College/University degree in Life Sciences or equivalent education/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.
• 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 SIV, RMV, COV onsite 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 participate on audits and inspections.

Skills

MS Office

English proficiency

Multitasking

Communication

Teamwork

Travel readiness

Driver's license

Education

College/University degree in Life Sciences

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.
• 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.