Our FSO department in Portugal is looking for a CRA I / II to manage clinical studies principally in Oncology, Hematology and Immunology. Home based in Porto area. Main Responsibilities Clinical site monitoring: conducts routine, pre‐study, initiation, and close‐out visits, ensuring full compliance with project plans. Site and patient protection: ensures informed consent, protocol adherence, and regulatory compliance to safeguard study participants. Data quality oversight: performs source document verification, CRF review, and manages data queries to ensure accuracy and completeness. Operational site management: prepares trip reports, ensures audit readiness, manages study files, coordinates with vendors, and uses resources efficiently. Safety reporting: tracks and follows up on Serious Adverse Events (SAEs), supporting report and narrative preparation. Extended support activities: feasibility assessments, QC visits, EC submissions, budget support, training/mentoring of new staff, and local project coordination. Cross‐functional communication & logistics: liaises with internal teams, manages study materials, and travels as required. Qualifications required University Master's degree in healthcare or similar. Basic understanding of the clinical trial process and foundational knowledge of applicable regulatory guidelines. Fluency in both English and the local office language, in written and verbal communication. Experience (Minimum Required) Mandatory 1 year minimum of experience as CRA. Understanding of Regulatory Guidelines. Good computer skills with good working knowledge of a range of computer packages. EEO & Accommodations request here. #J-18808-Ljbffr