Clinical Research Associate II (Medical)

TL;DR

Clinical Research Associate II (Medical): Monitoring and managing the progress of clinical studies at investigative sites with an accent on protocol compliance, ICH-GCP standards, and regulatory reporting. Focus on overseeing site activities, identifying potential study risks, and ensuring high-quality data collection in Oncology and Rare Disease trials.

Location: Remote, must be based in Hungary with domestic travel (up to 50-60%).

Company

A CRO integrating clinical trial execution with deep scientific knowledge and advanced data sciences, focusing on Oncology and Rare Disease.

What you will do

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations.
• Coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
• Conduct pre-study and initiation visits.
• Identify potential study risks and propose effective mitigation solutions.

Requirements

• Life science degree and/or equivalent experience.
• 2+ years of experience as a CRA in a CRO or pharmaceutical/biotech industry.
• Fluency in English and Hungarian.
• Availability for domestic travel (approximately 50-60% travel commitment).

Nice to have

• Experience in oncology monitoring.
• Experience with study start-up activities.

Culture & Benefits

• High CRA retention rates compared to industry averages.
• Manage a lower than average number of protocols to become a protocol expert.
• Reasonable travel expectations to ensure a better work-life balance.
• Ability to have direct influence and impact within a smaller CRO environment.
• Supportive direct line management.