Europe CRA: Remote & Onsite Clinical Monitoring

About the Role(s)

• Clinical Research Associate I/II
• Support/conduct site management through remote and supervised onsite visits (initiation, monitoring, and close‑out) in compliance with SOPs, protocol, and GCP.
• Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance.
• Assist or lead query resolution, safety reviews, and adverse event follow‑up throughout the study lifecycle.
• Support/conduct site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support.
• Maintain accurate, timely, and complete TMF documentation, requesting updates as required.
• Provide day‑to‑day operational support to Senior CRA and Lead CRAs.
• Participate in training, study meetings, and CRA development activities.

• Act as subject‑matter expert, mentor, coach, and/or provide performance feedback to manager for peers.
• Assist with selection, hiring, training, and supervision of CRAs as needed. Perform co‑monitoring and training visits with CRAs.
• Act as first escalation point for the resolution of site/patient issues or to address Sponsor concerns.
• Represent Director or Manager in BD initiatives with a site monitoring focus.
• May be assigned Lead CRA role and manage monitoring services for a group of projects and/or CRAs.
• Oversee overall integrity of the study and promote positive relationships with sites.
• Ensure SOPs to optimize patient recruitment, guiding site teams on inclusion/exclusion criteria.

• CRA I – minimum 1 year experience and Honours Bachelor Degree.
• CRA II – minimum 2 years experience and Honours Bachelor Degree.
• Sr. CRA – minimum 3 years experience and Honours Bachelor Degree.

• Compensation varies by seniority, location, and candidate experience.
• Full‑time permanent roles include a base salary plus performance‑based bonus, along with health, dental, RRSP matching, and more.
• Contact the TA team for more details.

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