Remote Dutch CRA Biotech Trials Phase I-III

KCR Placement; Utrecht; Hybrid; EUR 52,000 - 78,000; Full time

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme (

LifeWorks

Job summary

ICON plc is seeking an experienced Clinical Research Associate for a fully remote role based in the Netherlands. You will monitor Phase I-III trials, ensure regulatory compliance, and manage site visits across biotech sponsors.

Candidates should hold a life science degree, have 2+ years CRA experience in CRO/Pharma, and be fluent in Dutch and English, with a valid driver's license and willingness to travel within the Netherlands.

Qualifications

• Life science degree or equivalent.
• 2+ years experience as a CRA with CRO/Pharma exposure.
• Understanding of clinical trial processes and regulatory standards.

Responsibilities

• Manage clinical studies in the Netherlands for biotech sponsors.
• Monitor Phase I-III trials per ICH-GCP/regulations.
• Conduct site qualification, initiation, monitoring, close-out visits.

Skills

Life science degree or equivalent

2+ years CRA experience

Regulatory knowledge

Excellent communication

Organization and problem-solving

Clinical trial systems

Dutch & English fluency

Willingness to travel Netherlands

Driver's license

Education

Life science degree or equivalent

Tools

Clinical trial systems and tools

Job description

ICON plc is seeking an experienced Clinical Research Associate for a fully remote role based in the Netherlands. You will monitor Phase I-III trials, ensure regulatory compliance, and manage site visits across biotech sponsors.

Candidates should hold a life science degree, have 2+ years CRA experience in CRO/Pharma, and be fluent in Dutch and English, with a valid driver's license and willingness to travel within the Netherlands.