Experienced Clinical Research Associate (Level I/II) - FSP - Multi Therapeutics

This role focuses on monitoring clinical trial sites and coordinating site management for a single sponsor. Day to day, the work includes remote or in-person visits, checking that sites follow the approved protocol, regulatory requirements, ICH-GCP, and company procedures, and keeping trial records in good order. It also involves using a risk-based monitoring approach, reviewing source and case report data, checking investigational product records, writing visit reports and letters, and escalating issues when needed. The advert names root cause analysis, critical thinking, problem-solving, source data review, source data verification, and case report form review as part of the work. It asks for an experienced Clinical Research Associate at Level I or II, but does not give a specific degree or other qualification in the text provided. No language requirement is stated. The position is full-time and remote, with a standard Monday to Friday schedule and an office-based environmental setting noted in the advert. It would suit someone who can work independently with investigators and help keep studies compliant, audit-ready, and reliable.