Clinical Research Associate II
- Quebec, QC, Canada
$98,000 to $120,000 CAD / year · Full-time
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Job details
- Pay
- $98,000 to $120,000 CAD / year
- Job type
- Full-time
- Posting language
- English
- Posted
Original job description
Company Description
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.
Job Description
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.
More about this job
Responsibilities
The Clinical Research Associate II is responsible for conducting onsite monitoring visits and ensuring the quality of clinical study data. They manage site communications, perform source document verification, and support project teams with study progress and regulatory submissions.
Requirements
Candidates must hold a college or university degree in Life Sciences and possess independent onsite monitoring experience in North America. Proficiency in English and French is required, along with the ability to travel and manage Phase II/III clinical trial monitoring tasks.
Skills
- Clinical monitoring
- CRF review
- Source document verification
- Query resolution
- Site management
- Feasibility research
- Regulatory documentation
- Phase II clinical trials
- Phase III clinical trials
- Communication
- Problem-solving
- Multitasking
- MS Office
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Healthcare
Keywords
- Clinical Research Associate
- Contract Research Organization
- Clinical Trials
- Monitoring Visits
- CRF
- Source Document Verification
- Phase II
- Phase III
- Regulatory
- Life Sciences
- Site Management
- Feasibility
- MS Office
- Clinical Research