Senior Clinical Monitoring CRA II – Remote/Travel-Ready

Syneos Health

Amsterdam

On-site

EUR 60,000 - 85,000

Full time

14 days+

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Job summary

Syneos Health in Amsterdam, Netherlands is seeking a CRA II to oversee site monitoring activities across the drug development lifecycle. You will perform qualification, initiation, interim monitoring, and close-out visits (on-site or remote) to ensure protocol and regulatory compliance.

You will verify informed consent, protect data confidentiality, and conduct source document reviews with timely query resolution.

Qualifications

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
  • Knowledge of Good Clinical Practice/ICH Guidelines and other regulatory requirements.
  • Excellent communication, presentation and interpersonal skills.
  • Ability to manage required travel of up to 75% on a regular basis.

Responsibilities

  • Performs site qualification, initiation, monitoring, management and close-out visits (on-site or remote) ensuring regulatory compliance.
  • Verifies informed consent process and protects subject confidentiality and data integrity.
  • Conducts source document review, data checks, query resolution, and supports data capture and ISF/TMF reconciliation.
  • Manages IP inventory, labeling, and storage in line with protocol and regulatory requirements.
  • Attends Investigator Meetings and sponsor meetings; supports audit readiness and risk-based monitoring.
  • Maintains up-to-date knowledge of ICH/GCP Guidelines and local regulations.

Skills

Excellent communication
Interpersonal skills
Strong computer skills
Travel readiness

Education

Bachelor’s degree or RN in related field

Job description

Syneos Health in Amsterdam, Netherlands is seeking a CRA II to oversee site monitoring activities across the drug development lifecycle. You will perform qualification, initiation, interim monitoring, and close-out visits (on-site or remote) to ensure protocol and regulatory compliance.

You will verify informed consent, protect data confidentiality, and conduct source document reviews with timely query resolution.

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