Clinical Research Associate II

The company is a specialized CRO focusing on oncology and rare diseases, integrating clinical trial execution with scientific and data sciences, offering a supportive culture with high CRA retention, and providing opportunities for influence and growth.

Location: Hungary

Responsibilities

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations.
• Coordinate activities required to set up and monitor a study, including identifying investigators, preparing regulatory submissions, and conducting pre-study and initiation visits.

Requirements

• Life science degree and/or equivalent experience.
• At least 2 years as a CRA in a CRO or pharmaceutical/biotech industry or relevant experience.
• Availability for domestic travel including overnight stays, with potential international travel for senior positions.
• Excellent communication and organizational skills.
• Client-focused approach.
• Fluency in English and Hungarian.
• Oncology monitoring experience is a plus.