Clinical Trial Manager

Oxford Global Resources; Madrid; Presencial; EUR 50.000 - 80.000; 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 role involves leading clinical activities, ensuring compliance with regulations, and managing trial logistics. Join a fast-moving team focused on innovative cancer therapies and contribute to a transformational oncology program.

Formación

• Proven experience as a Clinical Trial Manager, preferably 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 and oversee first-in-human oncology trials.
• Ensure GCP and ICH E6(R2) compliance across all clinical activities.
• Manage trial budgets, vendor contracts, and timelines.

Conocimientos

Leadership

Communication

Problem Solving

Organizational Skills

Educación

Degree in Life Sciences

Degree in Healthcare

Degree in 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

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). This role offers the opportunity to be part of a first-in-human clinical program with studies launching in Spain and the U.S. You will work closely with senior leadership and external partners to contribute to innovative cancer therapies.

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 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 laboratories, vendors, and investigators for logistics and drug supply.
6. Participate in the preparation and review of trial documents such as protocols, ICFs, and patient materials.
7. Evaluate metrics and implement corrective actions for deviations.
8. Ensure documentation and compliance with regulatory requirements (EMA / FDA).
9. Manage trial budgets, vendor contracts, and timelines.
10. Represent the company in meetings and communications with investigators and sites.

Qualifications :

• Degree in Life Sciences, Healthcare, or Business Management.
• Proven experience as a Clinical Trial Manager, preferably 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.
• 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 with executive leadership and engage in 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