Clinical Research Associate II

Must have 2+ years of independent on-site monitoring experience

Experience in all types of monitoring visits, in phases I-III

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

For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.

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.

Build and maintain a good relationship with the site staff involved in the study conduct

Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits

Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations

Perform source data verification and follows up on data queries at site level; review and manage study risks on a site level

Ensure proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on sites

PSI is a leading Contract Research Organization with more than 30 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.