Clinical Research Associate II - Biotech - Netherland…

In this role you will contribute to Phase I–IV clinical trials within IQVIA Biotech’s EU Clinical Monitoring team. You will oversee site performance, ensure adherence to GCP/ICH, and coordinate monitoring activities with CTMs and Lead CRAs. You will train sites on study procedures, support data integrity, and manage investigator communications across studies. The position places you in Amsterdam, collaborating with cross-functional teams to drive study deliverables in a fast-paced, mission-driven environment. You will play a key role in mentoring junior CRAs and advancing high-quality clinical data and site partnerships.

• Participate in investigator recruitment and site evaluation to assess capability for study execution
• Coordinate initiation activities with sites and internal teams, including training on eCRF and EDC systems
• Monitor trials to ensure compliance with GCP/ICH and study procedures
• Resolve site file audit issues and ensure data quality through source data verification
• Prepare monitoring reports and maintain trial material accountability and inventory
• Review data quality via in-house CRF checks and on-site source verification; resolve data queries
• Serve as primary contact between IQVIA Biotech and investigators and manage study-related communications
• Assist with Investigator Meetings and attend relevant meetings to support study progress
• Ensure timely delivery of study deliverables and manage multiple trials in a matrix environment
• Conduct field evaluation visits and train CRAs and senior CRAs where needed
• Mentor junior CRAs and new joiners to the study footprint

• Minimum 1–2 years of on-site monitoring experience
• Strong knowledge of clinical research processes and medical terminology
• Excellent written and verbal communication in Dutch and English
• Ability to build productive cross-functional relationships and manage multiple priorities
• Ability to work independently in a matrix team environment
• Knowledge of GCP/ICH guidelines
• Proven ability to reason independently and propose clinical solutions

• communication skills
• relationship-building
• prioritization
• GCP/ICH knowledge
• on-site monitoring
• eCRF training and usage