Clinical Trials Data Entry Specialist - Madrid (Full-Time)

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

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.