Live opening · Posted 7 hours ago
The key details from the original listing.
Live timing from JobBeeper.
Description supplied by the original job listing.
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 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
Support and participate in audits and inspections
College/University degree in Life Sciences or an equivalent combination of education, training & experience
At least 1 year of independent on-site monitoring experience
Experience in all types of monitoring visits
Full working proficiency in English and Serbian
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 across the region
Valid driver’s license
Employment type
Full-time
Work arrangement
Yes
Recently tracked roles with full details and direct application links.