Clinical Trial Manager

Oxford Global Resources; Zaragoza; A distancia; EUR 40.000 - 70.000; Jornada completa

Descripción de la vacante

A leading biotech company is seeking a skilled Clinical Trial Manager (CTM) to oversee first-in-human oncology trials in Spain and the U.S. This role offers a unique opportunity to contribute to innovative cancer therapies and collaborate with executive leadership, focusing on developing a diverse pipeline of precision oncology therapeutics. If you're results-driven and possess strong compliance knowledge, this is your chance to transform cancer treatment in a supportive environment.

Formación

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

Responsabilidades

• Lead operational execution of clinical activities for oncology trials.
• Monitor trial progress, recruitment, and site performance.
• Ensure GCP and ICH compliance across all activities.

Conocimientos

Excellent communication

Leadership

Problem-solving

Organizational skills

Life Sciences knowledge

Clinical logistics knowledge

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

Company:

Oxford Global Resources

Position Overview:

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 participate in a first-in-human clinical program with studies launching in Spain and the U.S., contributing to innovative cancer therapies and 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., including CRO oversight.
3. Ensure GCP and ICH E6(R2) compliance across all activities.
4. Monitor trial progress, recruitment, site performance, sample tracking, eCRF data entry, and site documentation.
5. Coordinate with laboratories, vendors, and investigators for logistics and drug supply.
6. Prepare and review trial documents such as protocols, ICFs, and patient materials.
7. Evaluate metrics and implement corrective actions for deviations.
8. Ensure regulatory compliance (EMA/FDA) and manage trial budgets, vendor contracts, and timelines.
9. 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, ideally in oncology or early-phase trials.
• Strong knowledge of GCP, ICH, FDA/EMA regulations, and clinical 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 development, contributing to innovative biotech solutions. 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