Senior Clinical Research Associate
- Calgary, AB, 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
The Senior Clinical Research Associate will conduct onsite monitoring visits, perform CRF reviews, and ensure source document verification. They will also manage site communications, support regulatory submissions, and participate in audits and inspections.
Requirements
Candidates must hold a college or university degree in Life Sciences and possess independent on-site monitoring experience in Phase II and/or III clinical trials. Proficiency in English and French is essential, along with the ability to travel and a valid driver's license.
Skills
- Clinical research
- On-site monitoring
- CRF review
- Source document verification
- Query resolution
- Site management
- Regulatory documentation
- Feasibility research
- Audit preparation
- Inspection support
- Oncology
- MS Office
- Multitasking
- Problem-solving
- Communication
- Collaboration
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
Keywords
- Clinical Research Associate
- Contract Research Organization
- Monitoring visits
- SIV
- RMV
- COV
- CRF
- Source document verification
- Query resolution
- Site management
- Feasibility research
- Regulatory
- Audits
- Inspections
- Life Sciences
- Phase II
- Phase III
- Oncology
- MS Office
- Clinical studies
- Therapeutic indications