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 all types of onsite monitoring visitsBe involved in study startup and feasibility researchPerform 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 progressSupport regulatory team in preparing documents for study submissions

QualificationsCollege/University degree in Life Sciences or an equivalent combination of education, training & experience2 years of independent on-site monitoring experience in the United States requiredExperience in all types of monitoring visits in Phase II / IIIExperience in Oncology is preferredFull working proficiency in EnglishProficiency in MS Office applicationsAbility to plan and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travel

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.