Senior Clinical Research Associate – Netherlands

IQVIA LLC; Amsterdam; On-site; EUR 43,000 - 65,000; Full time

Job summary

IQVIA Biotech in the Netherlands seeks an experienced Clinical Monitor to participate in Phase I–IV trial monitoring, site evaluations, and initiation visits. The role ensures compliance with GCP/ICH guidelines and maintains strong coordination with the Clinical Trial Manager and Lead CRA.

Ideal candidates have 1–2 years of onsite monitoring experience, excellent communication skills in Dutch and English, and the ability to manage multiple trials in a matrix team environment.

Qualifications

• Minimum of 1–2 years of onsite monitoring experience.
• Strong knowledge of the clinical research process.
• Knowledge of Good Clinical Practices (GCP) and ICH guidelines.
• Proficient in Dutch and English communication.

Responsibilities

• Participates in investigator recruitment and site evaluation visits.
• Performs site initiation, monitoring, and close-out visits.
• Ensures study activities comply with GCP/ICH and sponsor procedures.
• Communicates with CTM/Lead CRA to ensure adherence to study requirements.
• Mentors junior CRAs and supports field training.

Skills

Clinical research

Onsite monitoring

GCP/ICH knowledge

Dutch language

English language

Communication

Tools

eCRF

EDC system

Job description

IQVIA Biotech in the Netherlands seeks an experienced Clinical Monitor to participate in Phase I–IV trial monitoring, site evaluations, and initiation visits. The role ensures compliance with GCP/ICH guidelines and maintains strong coordination with the Clinical Trial Manager and Lead CRA.

Ideal candidates have 1–2 years of onsite monitoring experience, excellent communication skills in Dutch and English, and the ability to manage multiple trials in a matrix team environment.