Clinical Research Associate I – Remote/On‑site Monitoring

About the role

Join a global CRO team that supports leading pharmaceutical and biotech companies across more than 100 countries. As a Clinical Research Associate I you will conduct remote and on‑site monitoring visits, ensuring trials follow the approved protocol, ICH‑GCP guidelines and regulatory requirements.

Key responsibilities

• Perform risk‑based monitoring of investigator sites, applying root‑cause analysis and corrective actions.
• Verify data accuracy through source data verification (SDR), source data review (SDV) and case report form (CRF) checks.
• Assess investigational product inventory and documentation.
• Document observations in reports and letters, escalating deficiencies to clinical management.
• Maintain regular communication with sites to confirm protocol compliance and timely data entry.
• Participate in investigator payment processing and site initiation/close‑out activities.
• Support investigator meetings and assist in identifying qualified sites.

Required profile

• Strong understanding of clinical trial processes and regulatory standards.
• Ability to apply critical thinking and problem‑solving skills to site issues.
• Excellent written communication for timely reporting.
• Detail‑oriented with a focus on audit readiness.

Required skills

• Knowledge of ICH‑GCP guidelines.
• Experience with source data verification (SDR) and source data review (SDV).
• Familiarity with investigational product handling and documentation.

What we offer

• Opportunity to work on diverse global clinical trials.
• Collaborative environment with experienced project teams.
• Professional development in clinical monitoring and site management.