Clinical Research Associate II
PSI CRO Open At a glance
Junior role at PSI CRO. Remote, Canada · full-time · CA$98,000–CA$120,000 base.
remoteroles summary, based on the employer's posting.
What you'll do
- Conduct and document on-site monitoring visits across different clinical studies
- Review case report forms and source records, then resolve queries
- Manage site communications and coordinate with internal support teams and vendors
- Track study progress with project teams and contribute to feasibility work
- Help prepare regulatory documents for study submissions and support study startup when needed
What you bring
- A college or university qualification in life sciences, or equivalent education, training and experience
- Independent on-site monitoring work in North America, including Phase II or III visits
- Professional working fluency in both English and French
- Working knowledge of MS Office and a valid driver’s license
Who this fits
This role suits someone with independent monitoring experience who wants exposure to different therapeutic areas. You’ll need to travel and hold a valid driver’s license.
From the employer
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.
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
- 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
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
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