Clinical Research Associate II (Oncology)

TL;DR

Clinical Research Associate II (Oncology): Monitoring and managing clinical study progress at investigative sites with an accent on protocol compliance, regulatory standards, and site management. Focus on ensuring high-quality data collection, mitigating study risks, and maintaining strong relationships with investigators in the Netherlands.

Location: Must be based in the Netherlands. This is a remote-based position with required domestic travel to sites.

Company

hirify.global is a specialized CRO integrating clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences, with a strong focus on oncology and rare diseases.

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, and ICH-GCP standards.
• 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.
• Maintain clear communication with project teams and site staff.

Requirements

• Must be based in the Netherlands.
• Life science degree or equivalent experience.
• Minimum 2 years of experience as a CRA in a CRO or pharmaceutical/biotech industry.
• Fluency in English and Dutch.
• Availability for domestic travel (approximately 50-60% commitment).
• Strong understanding of ICH-GCP and clinical research regulations.

Nice to have

• Oncology monitoring experience.
• Experience with study start-up activities.
• Proficiency in French.

Culture & Benefits

• High CRA retention rates compared to industry averages.
• Supportive direct line management and collaborative team environment.
• Lower than average number of protocols per CRA.
• Focus on work-life balance with reasonable travel expectations.
• Opportunity to have influence and impact within a smaller CRO environment.