Clinical Trial Manager

Oxford Global Resources; Lugo; A distancia; EUR 70.000 - 110.000; Jornada completa

Descripción de la vacante

Oxford Global Resources is seeking a Clinical Trial Manager for an oncology project, offering a unique opportunity to lead first-in-human trials in Spain and the U.S. The role involves overseeing clinical activities, ensuring compliance, and managing relationships with external partners in a fast-paced biotech environment.

Servicios

Transformational oncology program involvement

Fast-moving, innovative biotech environment

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, and clinical trial logistics.
• Experience managing CROs, sites, vendors, and cross-functional teams.

Responsabilidades

• Lead the operational execution of clinical activities.
• Oversee first-in-human oncology trials in Spain and the U.S.
• Ensure GCP and ICH E6(R2) compliance across all activities.

Conocimientos

Communication

Leadership

Problem-Solving

Organization

Adaptability

Educación

Background in Life Sciences, Healthcare, or Business Management

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 the development of innovative cancer therapies, working closely with senior leadership and external partners.

Key Responsibilities

1. Report directly to the Chief Medical Officer (CMO) and lead the operational execution of clinical activities.
2. Oversee first-in-human (FIH) oncology trials in Spain and the U.S., with external CRO oversight.
3. Ensure GCP and ICH E6(R2) compliance across all clinical activities.
4. Monitor trial progress, recruitment metrics, site performance, sample tracking, eCRF data entry, and site-level documentation.
5. Coordinate with central laboratories, vendors, and investigators for clinical logistics and drug supply.
6. Participate in the preparation and review of key trial documents: protocols, ICFs, patient materials, etc.
7. Evaluate metrics and create corrective action plans to address deviations.
8. Ensure timely documentation and adherence to regulatory requirements (EMA / FDA).
9. Prepare and monitor trial budgets, vendor contracts, and operational timelines.
10. Represent the company in investigator meetings, study team meetings, and site communications.

Requirements

• Background 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 environment.
• 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