Clinical Trial Manager (CTM) – Oncology Biotech Project Location: Remote / Europe-based (with occasional travel) Contract Type: Permanent direct with Biotech Company Start Date: Immediate or asap Oxford Global Resources is seeking a highly motivated Clinical Trial Manager (CTM) to join a cutting-edge global biotech company focused on developing a diverse pipeline of precision oncology therapeutics targeting the Tumor Microenvironment (TME). The position offers the opportunity to be part of a first-in-human clinical program, with studies launching in Spain and the U.S. This is a unique opportunity to contribute to the early-stage clinical development of innovative cancer therapies, working closely with senior leadership and external partners. Key Responsibilities * Report directly to the Chief Medical Officer (CMO) and lead the operational execution of clinical activities. * Oversee first-in-human (FIH) oncology trials in Spain and the U.S., with externalized CRO oversight. * Ensure GCP and ICH E6(R2) compliance across all clinical activities. * Monitor trial progress, recruitment metrics, site performance, and CRO deliverables. * Supervise sample tracking, eCRF data entry, and site-level documentation. * Coordinate with central laboratories, vendors, and investigators for clinical logistics and drug supply. * Participate in the preparation and review of key trial documents: protocols, ICFs, trial manuals, patient materials, etc. * Evaluate metrics and create corrective action plans to address deviations. * Ensure timely documentation and adherence to regulatory requirements (EMA/FDA). * Prepare and monitor trial budgets, vendor contracts, and operational timelines. * Represent the company in investigator meetings, study team meetings, and site communications. Requirements * Bachelor’s degree in Life Sciences, Healthcare, or Business Management. * Proven experience as a Clinical Trial Manager, ideally in oncology or early-phase trials. * Strong knowledge of GCP, ICH, FDA/EMA regulations, and clinical trial logistics. * Previous experience managing CROs, sites, vendors, and cross-functional teams. * Excellent communication, leadership, and problem-solving skills. * Highly organized, results-driven, and adaptable to dynamic environments. * Experience with clinical trial documentation systems and eCRFs. Why Join? * Be part of a transformational oncology program from early clinical development. * Contribute to cutting-edge precision medicine in a fast-moving, innovative biotech. * Collaborate closely with executive leadership, playing a strategic and hands-on role. * Engage in a high-impact, mission-driven environment with global scope. Interested? Apply now or contact Oxford Global Resources to learn more about this opportunity and how to join a biotech team redefining cancer treatment. Desired Skills and Experience #clinicalresearchjobs #clinicaltrialsjobs #projectmanagementjob