Assistant CRA

Overview

The Assistant Clinical Research Associate supports clinical study and site management activities remotely, working with CRAs and study Clinical Leads under SOPs and regulatory guidelines.

What you'll do

• Complete study and site management activities defined in assigned task matrices.
• Support site preparedness, pre-study assessments, and site start-up activities.
• Review and maintain essential documents, site information, and system records.
• Coordinate site supplies, vendor trackers, system access, training follow-up, and logistics.
• Support remote monitoring, centralized monitoring tool review, and missing data follow-up.
• Coordinate site payments, invoices, reconciliations, and administrative records.
• Perform assigned site management tasks and limited site contact activities.

What you'll need

• Bachelor's degree in a life science discipline, Registered Nursing certification, or equivalent qualification.
• 0 to 2 years of comparable experience.
• Basic medical or therapeutic-area knowledge and medical terminology.
• Ability to learn and apply ICH GCP, regulations, and company procedures.
• Strong communication, interpersonal, organizational, and time-management skills.
• Proficiency with computers and MS Office, with ability to learn relevant software.
• Excellent English language and grammar skills.

Details

• Remote role in Romania.
• Standard Monday-Friday work schedule.
• Occasional travel to clinics or hospitals may be required.