Sponsor-Dedicated CRA II: Site Monitoring Expert

IQVIA LLC; Amsterdam; Hybrid; EUR 52,000 - 72,000; Full time

Benefits offered by this job

Company car or mobility allowance

Technology bundle: laptop and iPhone

Career advancement programs

Home office setup support

Time-off policy and vacation days

Pension plan and insurance

Supplementary health insurance options

Job summary

IQVIA Netherlands is seeking a motivated Clinical Research Associate II to join our sponsor dedicated model. Based in the Netherlands, you will perform site monitoring visits and support trial execution in line with GCP/ICH.

You will work with site staff to manage recruitment, data queries, and ensure TMF/ISF accuracy. A Bachelor’s degree and 18 months on-site CRA experience are preferred, with fluent Dutch (C1) and English.

Qualifications

• Bachelor's Degree in scientific discipline or health care.
• Minimum of 18 months on-site CRA monitoring experience in CRO/pharma environment.
• Full professional fluency in Dutch (C1) and English; strong medical writing skills.
• Good knowledge of GCP/ICH regulatory requirements.
• Organizational and problem-solving skills.
• Exceptional interpersonal and cross-cultural communication skills to build strong partnerships.
• Collaborative mindset to work effectively with cross-functional global teams.

Responsibilities

• Perform site monitoring visits in line with contracted scope and GCP/ICH requirements.
• Drive site recruitment planning and track progress to support predictability.
• Administer protocol training and maintain regular communication with sites.
• Evaluate site practices for protocol compliance and quality.
• Escalate quality issues as appropriate.
• Manage progress of studies by tracking regulatory submissions, recruitment, CRF completion, data queries.
• May support start-up phase.
• Ensure site documents are filed in the TMF and ISF is maintained.
• Create and maintain documentation of site management and visit findings.
• Collaborate with study team members for project execution support.
• May support development of site-specific recruitment plans.

Skills

Dutch language

English language

Organizational skills

Problem-solving

Interpersonal skills

Cross-cultural communication

Collaborative mindset

Team collaboration

Education

Bachelor's Degree

Degree in scientific discipline/health care

Job description

IQVIA Netherlands is seeking a motivated Clinical Research Associate II to join our sponsor dedicated model. Based in the Netherlands, you will perform site monitoring visits and support trial execution in line with GCP/ICH.

You will work with site staff to manage recruitment, data queries, and ensure TMF/ISF accuracy. A Bachelor’s degree and 18 months on-site CRA experience are preferred, with fluent Dutch (C1) and English.