Netherlands-Based CRA I: Site Monitoring & Coordination

IQVIA LLC; Amsterdam; On-site; EUR 42,000 - 60,000; Full time

Benefits offered by this job

Company car or mobility allowance

Technology bundle (laptop, iPhone)

Career development programs

Home office setup support

Wellness reimbursement

Generous time-off & pension plan

Job summary

IQVIA Netherlands is seeking motivated Clinical Research Associate I to join our sponsor-dedicated model. The role focuses on site monitoring visits, regulatory compliance, and collaboration with Dutch site investigators and staff.

You will ensure protocol adherence, manage data quality, and support study start-up activities as needed. A Bachelor's degree and 6 months’ on-site monitoring experience are required, with fluent Dutch and English.

Qualifications

• Bachelor's degree in a scientific discipline or health care required.
• Minimum 6 months of independent, on-site monitoring experience within CRO/pharma.
• Full professional fluency in Dutch (C1) and English, including strong medical writing skills.
• Knowledge of GCP/ICH guidelines and applicable regulatory requirements.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, close-out) in line with scope of work and GCP/ICH requirements.
• Collaborate with sites to drive recruitment plans and ensure timely enrollment.
• Administer study training to sites and maintain regular communication with study personnel.
• Track regulatory submissions, approvals, recruitment, data query resolution, and TMF/ISF accuracy.
• Create and maintain documentation of monitoring visits and action plans.

Skills

Site monitoring

GCP/ICH knowledge

Dutch language

English language

Regulatory compliance

Problem solving

Education

Bachelor's degree in scientific discipline or health care

Job description

IQVIA Netherlands is seeking motivated Clinical Research Associate I to join our sponsor-dedicated model. The role focuses on site monitoring visits, regulatory compliance, and collaboration with Dutch site investigators and staff.

You will ensure protocol adherence, manage data quality, and support study start-up activities as needed. A Bachelor's degree and 6 months’ on-site monitoring experience are required, with fluent Dutch and English.