Clinical Trial Manager

Oxford Global Resources; Málaga; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

A leading biotech company is looking for a Clinical Trial Manager (CTM) to join their innovative oncology program. This role involves overseeing first-in-human clinical trials, ensuring compliance with regulatory standards, and leading cross-functional teams. You will play a crucial role in redefining cancer therapy while collaborating with executive leadership in a remote working environment, contributing to advancements in cancer treatment.

Servicios

Transformational oncology program participation

Collaborate with executive leadership

Innovative biotech advancements

Formación

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

Responsabilidades

• Lead the operational execution of clinical activities and oversee first-in-human trials.
• Ensure compliance with GCP and regulations, monitor trial progress, and manage budgets.
• Coordinate logistics, prepare trial documents, and represent the company in meetings.

Conocimientos

Leadership

Problem-solving

Communication

Organization

Educación

Degree in Life Sciences

Degree in Healthcare

Degree in 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

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). The role involves contributing to first-in-human clinical programs launching in Spain and the U.S., 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 CRO oversight.
3. Ensure GCP and ICH E6(R2) compliance across all clinical activities.
4. Monitor trial progress, recruitment, site performance, and sample tracking.
5. Manage eCRF data entry and site-level documentation.
6. Coordinate with laboratories, vendors, and investigators for logistics and drug supply.
7. Participate in the preparation and review of trial documents such as protocols, ICFs, and patient materials.
8. Evaluate metrics and develop corrective action plans for deviations.
9. Ensure documentation and regulatory compliance (EMA / FDA).
10. Manage trial budgets, vendor contracts, and timelines.
11. 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 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 development stages.
• Contribute to innovative biotech advancements in cancer treatment.
• Collaborate with executive leadership in a global environment.

Interested?

Apply now or contact Oxford Global Resources to learn more about this exciting opportunity to join a biotech team redefining cancer therapy.

Desired Skills and Experience: #clinicalresearchjobs #clinicaltrialsjobs #projectmanagementjob