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About the Role
As a Clinical Research Associate II at PSI, you will perform a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
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
Requirements
- 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
Location
- North America
Work Type
- Onsite
Education Level
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
Salary/Compensations
- CAD 98000 - CAD 120000 - yearly
About the Company
- 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.