Clinical Trial Manager

Oxford Global Resources; Palma de Mallorca; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

A leading biotech company is seeking a Clinical Trial Manager (CTM) to oversee first-in-human oncology trials. This permanent role offers a chance to work on innovative therapeutic pipelines, ensuring compliance with GCP and ICH regulations while managing cross-functional teams and vendor contracts. You will play a pivotal role in a global project, contributing to redefining cancer treatment.

Formación

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

Responsabilidades

• Lead operational execution of clinical activities and oversee trials.
• Monitor trial progress, recruitment metrics, and site performance.
• Ensure compliance with regulatory requirements and manage budgets.

Conocimientos

GCP

ICH E6(R2)

Oncology Trials

Clinical Trial Logistics

Project Management

Communication

Leadership

Problem-Solving

Budget Management

Educación

Degree in Life Sciences

Degree in Healthcare

Degree in Business Management

Herramientas

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

Company :

Oxford Global Resources

Position Overview :

We are 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 role provides a unique chance 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 external 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.

Required 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 Us :

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 global scope project.

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

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