Senior CRA (FSP) — Remote, Netherlands

IQVIA LLC; Amsterdam; Hybrid; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Excellent salary and benefits package

Company car or car allowance

Flexible working hours in a home-based

Stable workload, work-life balance

Career development opportunities

Work on cutting edge medicines

Job summary

IQVIA is seeking a Clinical Research Associate for the Netherlands in a single sponsor FSP model. You will manage monitoring across sites and drive recruitment plans, typically handling 1–2 protocols such as Oncology or Diabetes with dedicated line management.

Expect ~6–9 on-site days per month and a strong emphasis on quality and regulatory compliance. Join IQVIA’s global clinical research team and benefit from a stable role with potential for career development, flexible working arrangements,

Qualifications

• Have a degree in Life Sciences.
• Have at least 3 years of independent on-site monitoring experience.
• Be experienced in handling multiple protocols across a variety of drug indications with good time management skills.
• Have in depth GCP knowledge.
• Be flexible with the ability to travel nationwide.
• Hold a full and clean driving license.
• Possess strong communication, written and presentation skills are a must (must have fluency in English and Dutch language).

Responsibilities

• Site management and monitoring activities across the country.
• Work with sites to adapt, drive and track subject recruitment plan.
• Provide protocol and study training to the assigned sites.
• Create and maintain monitoring visit reports and action plans.
• If appropriate, co-monitor, train and mentor junior members of the team.
• Become part of our team.

Skills

On-site monitoring

GCP knowledge

Time management

English & Dutch fluency

Education

Life Sciences degree

Tools

Driving license

Job description

IQVIA is seeking a Clinical Research Associate for the Netherlands in a single sponsor FSP model. You will manage monitoring across sites and drive recruitment plans, typically handling 1–2 protocols such as Oncology or Diabetes with dedicated line management.

Expect ~6–9 on-site days per month and a strong emphasis on quality and regulatory compliance. Join IQVIA’s global clinical research team and benefit from a stable role with potential for career development, flexible working arrangements,