Requirements: English
Company: Oxford Global Resources
Region: Lugo , Galicia
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
- Bachelors 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
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