Senior CRA

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

 

• 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

 

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.