Clinical Trials Study Coordinator — Nephrology Data Lead

INCLIVA Biomedical Research Institute; España; On-site; EUR 35,000 - 48,000; Full time

Job summary

INCLIVA Biomedical Research Institute in Spain invites applications for a Research Technician (T3), Level 2 – 16 T, to support the PRIME-CKD project and clinical trials in the Nephrology Department under Dr. Górriz. The role focuses on planning, data handling and coordination within a multidisciplinary team.

The position requires nursing background, Master’s in Clinical Trials, and strong organizational skills; English knowledge is assessed for eligibility. It is a permanent, full‑time role.

Qualifications

• Master's degree in Clinical Trials (CT) with official recognition.
• Bachelor's Degree or Diploma in Nursing per MECES EQF standards.
• Experience in coordinating clinical trials and nephrology activities.
• Knowledge of English levels and related documentation.

Responsibilities

• Plan, organize, manage and coordinate project activities in nephrology.
• Maintain documentation and manage the project database.
• Prepare, curate and filter data from samples for genomic data platform.
• Attend project team meetings and support data integration.
• Ensure data quality and proper implementation of study tasks.

Skills

Clinical trial coordination

Nursing activities

Data management

Project meetings

Education

Master's in Clinical Trials

Bachelor's Degree in Nursing

Tools

Data management systems

Job description

INCLIVA Biomedical Research Institute in Spain invites applications for a Research Technician (T3), Level 2 – 16 T, to support the PRIME-CKD project and clinical trials in the Nephrology Department under Dr. Górriz. The role focuses on planning, data handling and coordination within a multidisciplinary team.

The position requires nursing background, Master’s in Clinical Trials, and strong organizational skills; English knowledge is assessed for eligibility. It is a permanent, full‑time role.