Clinical Research Associate II - Remote

Overview

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.

In Short

• Act as the main line of communication between the project team, sponsor, and the site.
• 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 timely definition and communication of subject recruitment targets.
• Perform source data verification and manage study risks at site level.
• Conduct site audit preparation visits and resolve findings.
• Participate in study site audits and client onsite visits as required.
• Support preparation of regulatory and ethics committee submission packages.
• Facilitate review and reconciliation of the study TMF on country and site levels.
• Assist Site Management Associates in maintaining study-specific tracking systems.

Requirements

• College/University degree in Life Sciences or equivalent.
• 2+ years of independent on-site monitoring experience.
• Experience in all types of monitoring visits, in phases I-III.
• Located in Central or West Coast of the United States preferred.
• Experience in Oncology and GI/GU highly preferred.
• Full working proficiency in English.
• Proficiency in MS Office applications.
• Ability to plan, multitask, and work in a dynamic team environment.
• Strong communication, collaboration, and problem-solving skills.
• Ability to travel up to 75%.

Benefits

• Opportunity to further develop your skills.
• Widen your therapeutic area experience.
• Become an expert in clinical research.