About this role
Here in Fortrea we are looking for an experienced CRA to join our miltisponsor team.
Responsibilities:
• Conduct site monitoring visits (initiation, routine, close-out) in line with SOPs, ICH-GCP, and study requirements • Ensure patient safety and protocol compliance, including informed consent and eligibility verification • Perform source data verification, resolve queries, and maintain high data quality and integrity • Maintain site documentation (ISF/eTMF) and ensure audit readiness at all times • Manage investigational product accountability and site supplies in line with protocol requirements • Collaborate with study teams to deliver milestones, prepare reports, and support timelines Requirements:
• Degree in Life Sciences, Nursing, or related field (or equivalent experience) • Minimum 2 years of independent clinical monitoring experience • Strong knowledge of ICH-GCP, clinical trial processes, and regulatory requirements • Ability to work independently, with good organisation and problem-solving skills • Experience with eClinical systems (e.g. CTMS, eCRF) and solid MS Office skills • Fluency in English and Romanian languages; willingness to travel (~60%)
Learn more about our EEO & Accommodations request here.