Clinical Research Associate II

As a CRA at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
Hybrid work with office in Warsaw.
You will:
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
Communicate with internal project teams regarding study progress
Participate in feasibility research
Support regulatory team in preparing documents for study submissions
Prepare and participate on audits and inspections
College/University degree in Life Sciences or an equivalent combination of education, training & experience
Experience in independent on-site monitoring in all types of visits is required
Experience in gastroenterology TA is required
Experience in neurology and oncology is a plus
Full working proficiency in Polish, English and in MS Office applications
Ability to travel and a valid driver's license

Employment type
Full-time

Work arrangement
Hybrid