Clinical Research Associate II
- Toronto, ON, 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
Conduct onsite monitoring visits and manage clinical study sites while ensuring quality standards are met. Coordinate with internal project teams and support regulatory document preparation for study submissions.
Requirements
Requires a college or university degree in Life Sciences and independent onsite monitoring experience in North America. Candidates must be proficient in English and French and possess a valid driver's license.
Skills
- Clinical monitoring
- CRF review
- Source document verification
- Query resolution
- Site management
- Regulatory documentation
- Feasibility research
- Project coordination
- MS Office
- Multitasking
- Problem-solving
- Communication
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
Keywords
- Clinical Research Associate
- Contract Research Organization
- Clinical Studies
- Therapeutic Indications
- Onsite Monitoring
- CRF
- Source Document Verification
- Query Resolution
- Site Communication
- Feasibility Research
- Regulatory Affairs
- Life Sciences
- Phase II
- Phase III
- MS Office
- Clinical Research