Senior CRA — On-site Monitoring & Site Partnerships

IQVIA; Amsterdam; On-site; EUR 60,000 - 80,000; Full time

Benefits offered by this job

Company car or flexible mobility allowance

Premium technology bundle

Career advancement training programs

Home office setup support

Comprehensive time-off policy

Robust pension plan

Optional health insurance reimbursement

Job summary

IQVIA in the Netherlands is seeking a Senior Clinical Research Associate to join their dynamic sponsor dedicated model. The role involves performing site monitoring visits, managing study progress, and ensuring compliance with GCP regulations.

Qualified candidates will have a Bachelor's degree in a scientific discipline, fluency in Dutch and English, and at least 3 years of on-site monitoring experience. The position offers excellent career advancement opportunities and a comprehensive benefits package.

Qualifications

• 3+ years of on-site monitoring experience as a CRA.
• Strong medical writing skills for reports.
• Experience within a CRO or pharmaceutical environment.

Responsibilities

• Perform site monitoring visits and ensure GCP compliance.
• Manage study progress and site documentation.
• Collaborate with study team members for execution support.

Skills

Fluency in Dutch

Fluency in English

Clinical research regulations knowledge

Organizational skills

Interpersonal communication skills

Problem-solving skills

Education

Bachelor's Degree in scientific discipline or health care

Tools

Laptop

iPhone

Job description

IQVIA in the Netherlands is seeking a Senior Clinical Research Associate to join their dynamic sponsor dedicated model. The role involves performing site monitoring visits, managing study progress, and ensuring compliance with GCP regulations.

Qualified candidates will have a Bachelor's degree in a scientific discipline, fluency in Dutch and English, and at least 3 years of on-site monitoring experience. The position offers excellent career advancement opportunities and a comprehensive benefits package.