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 in office 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 drivers 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.

Remote Work :

Yes

Employment Type :

Full-time

📌 Clinical Research Associate II (Toronto)
🏢 PSI CRO
📍 Toronto