Clinical Research Associate II

PSI CRO - Remote

Full-timeEstimated: $50,000 - $74,000 a year
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.


Conduct and report all types of onsite monitoring visits
Be involved in study startup
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
Supervise study activities, project timelines and schedules on a country level
Participate in quality control and compliance monitoring
Communicate with internal project teams regarding study progress
Participate in feasibility research
Support regulatory team in preparing documents for study submissions


College/University degree in Life Sciences or an equivalent combination of education, training & experience
At least 3 years of independent on-site monitoring experience in the United States
Experience in all types of monitoring visits in Phase II and/or III
Experience monitoring Oncology or Hematology sites required
Full working proficiency in English
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 and Valid driver’s license

Additional Information

All your information will be kept confidential according to EEO guidelines.