Clinical Trial Manager

Role: Clinical Trial Manager (CTM) supporting U.S. Clinical Operations in biopharma, focusing on site management, monitoring, and trial execution for cancer immunotherapy programs targeting PRAME. Responsibilities: oversee site feasibility, initiation, engagement, regulatory submissions, monitoring activities, and data quality; develop operational plans and training materials; guide CRAs and manage protocol deviations; ensure compliance with GCP, FDA, EMA, and company SOPs. Requirements: bachelor’s degree in life sciences, nursing, or related field; 2+ years’ on-site clinical monitoring and CTM experience within biotech/pharma; strong knowledge of clinical trial regulations and systems (CTMS, eTMF); experience managing oncology trials preferred. HighValue: oncology, immunotherapy, PRAME target, biologics, TCR T-cell therapies, TCR bispecifics, global trials, trial management, regulatory compliance, remote work with up to 50% travel.