CRA II: Field Monitoring & Study Coordination (Netherlands)

IQVIA LLC; Amsterdam; On-site; EUR 60,000 - 85,000; Full time

Benefits offered by this job

Car or mobility allowance

Annual wellness reimbursement

Career development opportunities

Job summary

IQVIA is seeking a Clinical Research Associate based in the Netherlands to conduct on-site monitoring visits and ensure study data is reported per protocol and regulatory guidelines. You will collaborate with sites to manage recruitment, training, and ongoing expectations.

The role requires at least 1 year of on-site CRA experience, Dutch at C1 level or above, and strong English communication. You will ensure TMF/ISF adherence and support cross-functional study teams as needed.

Qualifications

• Bachelor's degree in scientific discipline or health care is required.
• At least 1 year of on-site monitoring experience as a CRA.
• Dutch proficiency at C1 level or above is a must.
• Written and verbal communication skills including good command of English.
• Good knowledge of applicable clinical research regulatory requirements (GCP/ICH).

Responsibilities

• Perform site monitoring visits in accordance with scope and regulatory requirements (GCP/ICH).
• Drive and track subject recruitment plans to enhance predictability.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for protocol conduct and regulatory adherence.
• Track regulatory submissions, recruitment, CRF completion, and data queries.
• Maintain TMF and ISF documentation in line with regulatory needs.
• Create and maintain site management documentation and visit reports.
• Collaborate with study team for project execution support.

Skills

Communication skills

Dutch language proficiency

GCP/ICH knowledge

Education

Bachelor's degree in scientific discipline or health care

Job description

IQVIA is seeking a Clinical Research Associate based in the Netherlands to conduct on-site monitoring visits and ensure study data is reported per protocol and regulatory guidelines. You will collaborate with sites to manage recruitment, training, and ongoing expectations.

The role requires at least 1 year of on-site CRA experience, Dutch at C1 level or above, and strong English communication. You will ensure TMF/ISF adherence and support cross-functional study teams as needed.