Clinical Research Associate II
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Posted by PSICRO on the hiring system it uses for its careers page; applications go straight to the company.
Can I apply?
- Full-time
- Remote from Canada
- Work permit not stated
- Requires English + French
Remote Clinical Research Associate II role based in Québec City, QC, Canada, with onsite monitoring visits and site management for clinical studies.
Requires a Life Sciences degree (or equivalent experience), independent on-site monitoring experience in North America, and Phase II/III monitoring experience.
Requires full working proficiency in English and French, and a valid driver's license with ability to travel.
No salary is listed; full-time type comes from the ATS tag only.
From the posting
- workplace
ATS workplace type: remote
- locations
ATS location: Remote - Québec City, QC, Canada
- employment types
full_time
- remote eligible countries
Remote - Québec City, QC, Canada
- seniority
Clinical Research Associate II
- job function
Conduct and report all types of onsite monitoring visits
- role family
Clinical Research Associate II
- skills
Proficiency in MS Office applications
- skills
Perform CRF review, source document verification and query resolution
- languages required
Full working proficiency in English and French.
- education required
College/University degree in Life Sciences or an equivalent combination of education, training & experience
- actionable
Conduct and report all types of onsite monitoring visits
- scam risk
Ability to travel
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.
Seen on
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