Primarily a training and development role, this position supports and observes clinical site monitoring services both inhouse and in the field whilst developing CRA skills and knowledge. This role has exposure and training in all aspects of the clinical site monitoring services while providing monitoring and site management activities for full-service studies, assessing protocol, SOP, and regulatory compliance.

As a CRA II, you will monitor multiple Phase I, II, III & IV clinical trial sites across different therapeutic areas. The CRA is the main sponsor representative, providing key project updates, collaborating with the team, and developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely. You will review source to CRF/eCRF, ensuring patient safety and data integrity. You will also oversee the sites' adherence to GCP/ICH practices.

This contract position ensures that data collected for clinical studies is accurate, plausible, and traceable to source documentation, assisting in site management, and clinical study materials development.

Oversee multiple oncology trials, ensuring high-quality execution. Provide leadership and mentorship to junior flex team members. Act as Lead SM, training and guiding other Site Managers on study protocols. Develop essential study start-up documents, including SIV agendas. Represent Site Managers and Lead Trial Managers (LTMs) in key meetings.