Senior Clinical Research Associate
- Vancouver, BC, Canada
$120,000 to $150,000 CAD / year · Full-time
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Job details
- Pay
- $120,000 to $150,000 CAD / year
- Job type
- Full-time
- Posting language
- English
- Posted
Original job description
Company Description
PSI is a leading Contract Research Organization with 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 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 SIV, RMV, COV onsite monitoring visits
- 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
- Prepare and particiapte on audits and inspections
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology is a plus
- Full working proficiency in English and French is essential.
- 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 and report onsite monitoring visits, review case report forms, verify source documents, resolve queries, and manage communication with clinical sites. Coordinate with internal teams and vendors, support feasibility research and regulatory submissions, and participate in audits and inspections.
Requirements
A college or university degree in life sciences, or an equivalent combination of education, training, and experience, is required, along with independent onsite monitoring experience and experience across monitoring visit types in Phase II and/or III trials. Full working proficiency in English and French, Microsoft Office proficiency, strong planning, communication, collaboration, and problem-solving skills, willingness to travel, and a valid driver’s license are required; oncology experience is an asset.
Skills
- Clinical Monitoring
- Site Management
- Source Document Verification
- CRF Review
- Query Resolution
- Site Communication
- Feasibility Research
- Regulatory Documentation
- Audit Preparation
- Inspection Preparation
- Oncology
- English Proficiency
- French Proficiency
- Microsoft Office
- Planning
- Multitasking
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
Keywords
- Clinical Research
- Contract Research Organization
- Clinical Research Associate
- Clinical Trials
- Clinical Monitoring
- Site Initiation Visit
- Routine Monitoring Visit
- Close-Out Visit
- Case Report Form
- Source Document Verification
- Query Resolution
- Site Management
- Feasibility Research
- Regulatory Submissions
- Audits
- Inspections
- Phase II
- Phase III
- Oncology
- Life Sciences
- Microsoft Office
- English
- French
- Travel
- Valid Driver’s License