Senior Clinical Research Associate

Job Description

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

Qualifications

• 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

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.