Data Entry

FUNDACION DE INVESTIGACION BIOMEDICA HOSPITAL 12 DE OCTUBRE; Spain; On-site; EUR 32,000 - 42,000; Full time

Job summary

FUNDACION DE INVESTIGACION BIOMEDICA HOSPITAL 12 DE OCTUBRE in Madrid seeks a Bachelor’s-level health sciences professional to support clinical trials, focusing on data collection, monitoring, and regulatory compliance. The role involves collaboration with investigators, trial coordinators, and the clinical team to ensure quality and patient safety.

You will participate in training, attend clinical sessions, manage data forms, and report adverse events under GCP guidelines.

Qualifications

• Bachelor’s degree in Health Sciences (Biology, Biotechnology, Pharmacy, or related health fields)
• Good Clinical Practice (GCP) R3 guidelines
• Experience in clinical trials sector or monitoring; oncology experience valued, research project involvement advantageous

Responsibilities

• Undertake all training required by the sponsor for each assigned clinical trial.
• Establish internal communication with investigators and trial coordinators to resolve enrolled patient queries.
• Take part in monitoring visits for assigned clinical trials.
• Complete data collection forms based on source documents and resolve queries.
• Collaborate in reporting serious adverse events in accordance with legislation and sponsor requirements.
• Attend the Unit’s clinical sessions and required trainings with the Head of the Clinical Research Unit.

Skills

GCP guidelines

Clinical trials experience

IT skills

Education

Bachelor’s degree in Health Sciences

Tools

Databases

Hospital management software

Job description

Organisation/Company FUNDACION DE INVESTIGACION BIOMEDICA HOSPITAL 12 DE OCTUBRE Research Field Biological sciences » Other Researcher Profile Other Profession Positions Bachelor Positions Application Deadline 12 Nov 2026 - 23:59 (Europe/Madrid) Country Spain Type of Contract Permanent Job Status Full-time Hours Per Week 37,5 Offer Starting Date 11 Nov 2026 Is the job funded through the EU Research Framework Programme? Other EU programme Is the Job related to staff position within a Research Infrastructure? No

Offer Description

DUTIES TO BE PERFORMED:

• Undertake all training required by the sponsor for each of the assigned clinical trials.
• Establish internal communication channels with investigators and/or trial coordinators to resolve queries regarding enrolled patients.
• Take part in monitoring visits for each assigned clinical trial.
• Complete the data collection forms for the assigned studies, based on the source documents, and resolve any queries.
• Collaborate with the trial coordinator in reporting serious adverse events occurring in a clinical trial, in accordance with current legislation and the sponsor’s requirements, following review and signature by the investigator.
• Attend the Unit’s clinical sessions, regular clinical research sessions and any training sessions required by the Head of the Clinical Research Unit.
• Academic Qualifications: Bachelor’s degree inHealth Sciences (Biology, Biotechnology, Pharmacy, or other related health fields )

Specific Requirements

• Specific training:Good Clinical Practice (GCP) R3 guidelines
• Experience: Experience in the clinical trials sector or clinical trial monitoring, including medical oncology and/or participation in research projects, will be an advantageIT skills: Databases, hospital management software.

Languages

ENGLISH Level Good

Work Location(s)

Number of offers available 2 Company/Institute FUNDACION BIOMEDICA HOSPITAL 12 DE OCTUBRE Country Spain State/Province MADRID City MADRID Postal Code 28041 Street AVDA DE CORDOBA S/N Geofield