Senior Clinical Research Associate — Sponsor‑Driven (NL)

IQVIA; United States; Remote; USD 57,000 - 85,000; Full time

Benefits offered by this job

Company car / mobility allowance

Technology bundle (laptop + iPhone)

Career advancement programs

Home office setup support

Generous PTO & flexible year-end leave

Pension plan & insurance

Supplementary health insurance options

Job summary

IQVIA in the Netherlands is seeking a motivated Senior Clinical Research Associate to join our Sponsor dedicated model. You will conduct site monitoring visits, drive patient recruitment plans, and ensure regulatory compliance across multiple sites, collaborating with global teams.

The role requires a Bachelor’s degree in a scientific field and at least 3 years of independent CRA on-site monitoring experience, with full professional fluency in Dutch and English, and strong medical writing

Qualifications

• Bachelor’s degree in a scientific discipline or health care.
• Minimum of 3 years on-site CRA monitoring experience.
• Full professional fluency in Dutch (C1) and English, including medical writing for reports.
• Strong knowledge of GCP and ICH guidelines.
• Excellent organizational and problem-solving abilities.
• Strong interpersonal and cross-cultural communication skills.
• Collaborative mindset to work with cross-functional global teams.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per contracted scope and GCP/ICH requirements.
• Drive subject recruitment plans in line with project needs to enhance predictability.
• Administer protocol and related study training to sites and maintain regular communication.
• Evaluate site practices for protocol conduct and regulatory adherence; escalate quality issues.
• Track regulatory submissions, recruitment, CRF completion, data queries; may support start-up.
• Ensure TMF/site documents are filed and ISF maintained per requirements.
• Create and maintain documentation of site management and visit findings with action plans.
• Collaborate with study team members for project execution support.
• May support development of site recruitment plans per site.

Skills

Dutch language fluency

English language fluency

Organizational skills

Problem-solving

Cross-cultural communication

Team collaboration

Education

Bachelor’s degree in scientific discipline or health care

Job description

IQVIA in the Netherlands is seeking a motivated Senior Clinical Research Associate to join our Sponsor dedicated model. You will conduct site monitoring visits, drive patient recruitment plans, and ensure regulatory compliance across multiple sites, collaborating with global teams.

The role requires a Bachelor’s degree in a scientific field and at least 3 years of independent CRA on-site monitoring experience, with full professional fluency in Dutch and English, and strong medical writing