Senior CRA – Sponsor‑Driven Clinical Trials & Growth

IQVIA LLC; Amsterdam; On-site; EUR 65,000 - 90,000; Full time

Benefits offered by this job

Company car or mobility allowance

Tech bundle (laptop + iPhone)

Job summary

IQVIA Netherlands is seeking a Senior Clinical Research Associate to join our Sponsor-dedicated model. This role is based in the Netherlands and focuses on site monitoring, regulatory compliance, and ongoing project support.

Ideal candidates hold a Bachelor’s degree in a scientific field, have at least 3 years of independent CRA experience in CRO/pharma, and are fluent in Dutch (C1) and English with strong medical writing skills.

Qualifications

• Bachelor's Degree in a scientific discipline or health care.
• Minimum 3 years of independent, on-site CRA monitoring experience in CRO/pharma.
• Fluent Dutch (C1) and English, with strong medical writing skills.

Responsibilities

• Perform site monitoring visits (initiation, monitoring, close-out) per GCP/ICH and contract.
• Lead site recruitment planning to meet project needs and improve predictability.
• Administer protocol training and maintain regular communication with sites.
• Track regulatory submissions, approvals, recruitment, CRF completion, and data queries.
• Escalate quality issues and ensure TMF/ISF alignment with regulatory requirements.
• Collaborate with cross-functional teams to support project execution.

Skills

Dutch language proficiency

English language proficiency

Interpersonal communication

Cross-cultural communication

Education

Bachelor's Degree in scientific discipline or health care

Tools

GCP knowledge

ICH guidelines

Job description

IQVIA Netherlands is seeking a Senior Clinical Research Associate to join our Sponsor-dedicated model. This role is based in the Netherlands and focuses on site monitoring, regulatory compliance, and ongoing project support.

Ideal candidates hold a Bachelor’s degree in a scientific field, have at least 3 years of independent CRA experience in CRO/pharma, and are fluent in Dutch (C1) and English with strong medical writing skills.