Clinical Trial Manager

Oxford Global Resources; Donostia/San Sebastián; A distancia; EUR 65.000 - 85.000; Jornada completa

Descripción de la vacante

A leading biotechnology company is seeking a Clinical Trial Manager (CTM) for oncology projects. This role offers the opportunity to manage innovative trials targeting the Tumor Microenvironment across Europe, ensuring compliance and leading diverse teams. Join a fast-paced environment that shapes the future of cancer treatment.

Servicios

Innovative oncology program

Collaboration with executive leadership

Global project engagement

Formación

• Proven experience as a Clinical Trial Manager, ideally in oncology or early-phase trials.
• Strong knowledge of GCP, ICH, FDA / EMA regulations.
• Experience managing CROs and cross-functional teams.

Responsabilidades

• Lead the operational execution of clinical activities.
• Oversee first-in-human oncology trials in Spain and the U.S.
• Prepare and monitor trial budgets and vendor contracts.

Conocimientos

Leadership

Communication

Problem-solving

Organizational skills

Educación

Degree in Life Sciences, Healthcare, or Business Management

Herramientas

Clinical trial documentation systems

eCRFs

Descripción del empleo

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) 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 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, 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, 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.

Qualifications

• 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.
• 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 a fast-moving, innovative biotech.
• Collaborate closely with executive leadership, playing a strategic and hands-on role.
• Engage in a project with a 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