Senior Clinical Research Associate

PSI CRO; Remote; CAD 70,000 - 90,000; Full time

Job summary

A leading Contract Research Organization is seeking a Senior CRA to ensure the quality and compliance of clinical research projects. This home-based role in Quebec involves conducting onsite monitoring visits, overseeing study activities, and maintaining stakeholder relationships. Candidates should have a College or University degree in Life Sciences, experience in Phase II/III monitoring, and proficiency in English and French. Join a company that values employee development and success.

Qualifications

• Experience in all types of monitoring visits in Phase II and/or III.
• Participation in clinical projects as a Lead/Senior Monitor.
• Experience in Oncology.

Responsibilities

• Conduct and report all types of onsite monitoring visits.
• Be involved in study startup.
• Perform CRF review, source document verification and query resolution.
• Be responsible for site communication and management.
• Supervise study activities, timelines, and schedules.

Skills

Full working proficiency in English and French

Communication skills

Collaboration skills

Problem-solving skills

Ability to plan and multitask

Education

College/University degree in Life Sciences

Tools

MS Office applications

Job description

PSI is a leading Contract Research Organization with more than 30 years in the industry /on the market, 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.

Job Description

As a Senior CRA you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Home-based in Quebec, Canada.

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Supervise study activities, timelines, and schedules on the country level
• Be a point of contact for in-house support services and vendors
• Be involved in quality control, such as compliance monitoring and reports review
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

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
• Participation in clinical projects as a Lead/Senior Monitor
• Experience in Oncology
• 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 (if applicable)

Additional Information

Make the right call andtake your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.