Remote Work Opportunity
Clinical Research Associate II
Deadline: Not specified
Short Summary
Clinical Research Associate II at PSI CRO. About the employer 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. Responsibilities As a Clinical Research Associate II at PSI you will enjoy a variety of…
Key Details
- Position / opportunity: Clinical Research Associate II
- Organization: PSI CRO
- Country / coverage: Canada
- Location: Québec City, QC, Canada
- Work arrangement: Remote
- Opportunity type: Remote work opportunities
- Sector: Health
- Compensation: Not specified
- Application deadline: Not specified by source
Description
About the employer
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.
Responsibilities
As a Clinical Research Associate II 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.
You will:
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
Qualifications
College/University degree in Life Sciences or an equivalent combination of education, training & experience
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
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.
Responsibilities
- As a Clinical Research Associate II 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.
- 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 / Eligibility
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
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
How To Apply
Select Apply now to complete the application for this position. Submit the documents requested in the application form.