Company Description

PSI is a leading Contract Research Organization with more than 25 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.

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 visitsPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team in preparing documents for study submissionsPrepare and particiapte on audits and inspections

Qualifications

 

College/University degree in Life Sciences or an equivalent combination of education, training & experienceIndependent on-site monitoring experienceExperience in all types of monitoring visits in Phase II and/or IIIExperience in Oncology is a plusFull working proficiency in English and French is essential.Proficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travelValid 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.