Study Coordinator - Data Entry

IBIMA Plataforma BIONAND; España; On-site; EUR 28,000 - 30,000; Full time

Job summary

IBIMA Plataforma BIONAND is seeking a Clinical Trials Coordinator for Translational Cancer Research, focusing on immunotherapy and epigenetics. The ideal candidate has demonstrable experience in the Clinical Trials sector and oncology trials, plus GCP/IATA certifications.

The position is based at Virgen de la Victoria University Hospital, 35 hours per week (8:00–15:00). Gross annual salary is €30,000 (€28,000 fixed + €2,000 variable); contract type is Permanent and tied to project duration.

Qualifications

• Demonstrated 1 year experience in Clinical Trials sector as Study Coordinator.
• Experience as Oncology Clinical Trials Coordinator.
• Certificates in GCP, IATA, Monitoring Masters, etc.
• Experience in Phase I Oncology Trials.
• High level English (B1-C1) or above.

Skills

Clinical Trials experience

Oncology trials coordination

GCP / IATA certificates

Phase I oncology trials

English language (C1)

Education

Medicine

Biochemistry

Pharmacy

Biology

Job description

Organisation/Company IBIMA Plataforma BIONAND Research Field Medical sciences » Health sciences Researcher Profile Other Profession Positions PhD Positions Application Deadline 21 Nov 2026 - 00:00 (Europe/Madrid) Country Spain Type of Contract Permanent Job Status Full-time Hours Per Week 35 Offer Starting Date 12 Nov 2026 Is the job funded through the EU Research Framework Programme? Other EU programme Reference Number 2026/256 Is the Job related to staff position within a Research Infrastructure? No

Offer Description

Information:

Reference: 2026/256

Research line description: Clinical-Translational Research in breast, prostate, gynecologic, digestive, and germ cell cancers.

Research line: IBIMA-B-05 TRANSLATIONAL RESEARCH IN CANCER IMMUNOTHERAPY AND EPIGENETICS

Principal Investigator: ANTONIO RUEDA DOMINGUEZ

Place of Work: IBIMA Bionand Platform - Located at Virgen de la Victoria University Hospital, 2nd Floor, Medical Oncology Clinical Trials Unit, clinical trial coordinators office - Phase 1

• Experience (demonstrable) in the Clinical Trials sector (Study Coordinator) of 1 year (1 point).
• Previous experience as an Oncology Clinical Trials Coordinator (0.5 points per year worked, maximum 1 point)
• Holding certificates for courses related to clinical trials and their implementation (GCP, IATA, Monitoring Masters, etc.) (0.5 points per course completed, maximum 2 points)
• Previous experience in Phase I Oncology Clinical Trials (0.5 points per year worked, maximum 2 points)
• High level of English. (B1 - 0.5 points and C1 - 1 point)

The above requirements must be accredited with an official certificate issued by the competent authority or a responsible declaration.

Specific Requirements

Degree holder/Graduate in the Biosanitary field: Medicine, Biochemistry, Pharmacy, Biology

Languages ENGLISH Level Excellent

Additional Information

• Hiring type: Scientific-Technical Activities Contract (art. 23 bis of the Science and Technology Law 14/2011)
• Category: Scientific - Technical Staff
• Weekly schedule: 35 hours (100%). Working hours from 8:00 a.m. to 3:00 p.m.
• Gross annual salary: €30,000
• Fixed salary: €28,000
• Variable salary: €2,000
• Estimated duration: The contract is tied to the duration of the project/activity/funding.