Senior Clinical Research Associate - Sponsor-Dedicated, NL

IQVIA Inc; Amsterdam; Hybrid; EUR 60,000 - 90,000; 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 vacation and leave options

Pension plan and insurance coverages

Supplementary health insurance option

Sign-on bonus up to €4,300

Job summary

IQVIA Netherlands is seeking motivated Senior Clinical Research Associate to join our Sponsor dedicated model. This role is based in the Netherlands and focuses on site monitoring, recruitment planning, and regulatory compliance with GCP/ICH guidelines.

The candidate should have a Bachelor’s degree in a scientific discipline or healthcare, at least 3 years of independent on-site CRA experience, and full professional fluency in Dutch and English.

Qualifications

• Bachelor's Degree in scientific discipline or health care.
• Minimum of 3 years of independent, on-site monitoring experience as a CRA within a CRO or pharmaceutical environment.
• Full professional fluency in Dutch (C1) and English, including strong medical writing skills for reports.
• Good knowledge of GCP and ICH guidelines.
• Organizational and problem-solving skills.
• Excellent interpersonal and cross-cultural communication to build partnerships with Dutch site investigators.
• Collaborative mindset to work with cross-functional global teams.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope of work and GCP/ICH requirements.
• Drive and track subject recruitment plan with sites to enhance predictability.
• Administer protocol training to sites and maintain regular communication with sites.
• Evaluate site practices for protocol conduct and regulatory compliance; escalate issues as needed.
• Manage study progress by tracking submissions, recruitment, CRF completion, data queries; may support start-up.
• Ensure site documents are filed in TMF and ISF maintained per GCP/local regs.
• Create and maintain documentation on site management and monitoring findings.

Skills

Dutch (C1)

English (C1)

On-site monitoring

Regulatory knowledge

Communication skills

Collaborative mindset

Education

Bachelor's Degree in scientific discipline or health care

Job description

IQVIA Netherlands is seeking motivated Senior Clinical Research Associate to join our Sponsor dedicated model. This role is based in the Netherlands and focuses on site monitoring, recruitment planning, and regulatory compliance with GCP/ICH guidelines.

The candidate should have a Bachelor’s degree in a scientific discipline or healthcare, at least 3 years of independent on-site CRA experience, and full professional fluency in Dutch and English.