Clinical Research Associate II (Oncology)

TL;DR

Clinical Research Associate II (Oncology) (Clinical Trials): Monitoring and coordinating oncology and other clinical studies at investigative sites with an accent on protocol compliance, site management, and risk mitigation. Focus on conducting monitoring visits, supporting study start-up activities, and ensuring accurate clinical trial documentation under ICH-GCP and applicable regulations.

Location: Remote-based in Belgium, primarily monitoring sites in Belgium with occasional support for sites in the Netherlands. Domestic travel, including overnight stays, may account for approximately 50–60% of the role.

Company

hirify.global is a CRO supporting life sciences organizations through integrated clinical trial execution, scientific expertise, laboratory services, and advanced data sciences, with a focus 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 according to protocols, SOPs, ICH-GCP, regulations, and applicable standards.
• Coordinate study set-up and monitoring activities, including investigator identification and regulatory submission preparation.
• Conduct pre-study and initiation visits and support ongoing site management.
• Identify study risks, develop mitigation solutions, and resolve site or project challenges.
• Collaborate with investigators, project teams, and clients to maintain study quality and outcomes.

Requirements

• Life science degree or equivalent experience.
• At least two years of CRA experience in a CRO, pharmaceutical, or biotech environment, or equivalent clinical research experience.
• Site management or equivalent clinical research experience.
• Fluency in English and Dutch is required.
• Excellent communication, organizational, conflict-resolution, and risk-management skills.
• Availability for domestic travel with overnight stays, including an expected travel commitment of approximately 50–60%.

Nice to have

• Oncology study management experience.
• Study start-up experience.
• French fluency.

Culture & Benefits

• Remote-based work with a manageable travel schedule.
• Lower-than-average protocol loads to support protocol expertise.
• Direct line-management support and opportunities to influence study delivery.
• Focus on quality of life, work-life balance, and collaborative working relationships.
• Opportunity to work within an integrated CRO combining clinical, scientific, laboratory, and data-science capabilities.