Clinical Research Associate II

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 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