Clinical Trial Data Entry

Description

We are seeking a **Clinical Trial Data Entry** professional to support the management and development of clinical studies at our center in **Las Palmas de Gran Canaria**. The selected candidate will join our **clinical trial coordination team**, closely collaborating with investigators, coordinators, monitors, and sponsors to ensure proper study management. Requirements * Education related to the **healthcare or scientific field**. * Prior experience in **clinical trials, clinical research, or data management** will be valued. * Organizational skills, attention to detail, and ability to work in a team. * Familiarity with clinical trial management platforms and **CRF/eCRF** will be valued. * Proficiency in English will be valued, especially for handling documentation and international study platforms. Main Responsibilities * Entering and updating **clinical data in CRF/eCRF and other sponsor platforms**, in accordance with established protocols and procedures. * Reviewing information and resolving/tracking **queries** related to entered data. * Preparing, organizing, and maintaining **study and patient documentation**. * Supporting the coordination team in managing and monitoring clinical trials. * Preparing necessary documentation and information for **monitoring visits**. * Assisting with **initiation, follow-up, and close-out visits** for studies. * Coordinating with investigators, coordinators, and monitors to ensure accurate and timely updates of study information. * Archiving and controlling documentation related to clinical trials. * Other support tasks typical of the **clinical research team**. Position Type: Full-time Work Location: On-site