Netherlands-based CRA II: Site Monitoring & Study Delivery

IQVIA Argentina; Amsterdam; On-site; EUR 52,000 - 72,000; Full time

Benefits offered by this job

Car or mobility allowance

Annual wellness reimbursement

Home office setup support

Pension plan and insurance

Job summary

IQVIA, based in the Netherlands, is seeking a Clinical Research Associate to perform site monitoring and manage study data in accordance with the protocol, GCP, ICH, and sponsor requirements. The role requires on-site work from the Netherlands and collaboration with study teams to ensure quality and regulatory adherence.

The candidate should have a Bachelor’s degree in a scientific field, at least 1 year of on-site CRA experience, and strong Dutch (C1) and English communication skills.

Qualifications

• Bachelor's Degree in a scientific discipline or health care is required.
• Minimum 1 year of on-site monitoring experience as a CRA.
• Dutch proficiency at C1 level or above is a must.
• Written and verbal communication skills including good command of English language.
• Good knowledge of GCP/ICH regulatory requirements.
• Good therapeutic and protocol knowledge as provided in company training.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in line with GCP/ICH guidelines.
• Drive and track subject recruitment plans to match project needs.
• Administer protocol and related study training to sites and maintain regular communication.
• Evaluate site practices for protocol conduct and regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion, data query generation and resolution; may support start-up.
• Maintain TMF/ISF documentation and site-related files.

Skills

Dutch proficiency (C1)

English communication

Education

Bachelor's Degree in scientific discipline or health care

Job description

IQVIA, based in the Netherlands, is seeking a Clinical Research Associate to perform site monitoring and manage study data in accordance with the protocol, GCP, ICH, and sponsor requirements. The role requires on-site work from the Netherlands and collaboration with study teams to ensure quality and regulatory adherence.

The candidate should have a Bachelor’s degree in a scientific field, at least 1 year of on-site CRA experience, and strong Dutch (C1) and English communication skills.