Clinical Trial Manager

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

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