Description
**What will you do in the team?**
Data management: Collect, organize, and maintain clinical and research data, ensuring the quality and accuracy of data entered into databases and management systems.
Clinical trial coordination: Facilitate the development and implementation of clinical trials, including preparation of documentation, participant follow-up, and management of monitoring visits.
Clinical support: Perform typical nursing functions, such as vital signs measurement, electrocardiograms, laboratory tests, and coordination of medical and laboratory visits.
Biological sample collection: Collect and process biological samples according to established protocols.
Data analysis: Evaluate data obtained from clinical trials, ensuring compliance with Good Clinical Practice (GCP) and relevant regulations.
Communication and collaboration: Collaborate with other members of the research team and communicate results.
**What do you need?**
We are seeking professionals who are highly motivated and passionate about helping others and giving their best.
**Education**:
Bachelor's/Degree in Nursing.
Master's in Clinical Trial Monitoring and Coordination (or similar).
**Experience**:
Minimum of 1 year of experience as a Nurse is desirable.
**Other skills and knowledge**:
Experience or training in the Clinical Trials Unit.
**Innovation, commitment to you, and customer support**
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At Sanitas, we welcome you with open arms. You will join an innovative team committed to its employees and focused on caring for and supporting customers. We offer a dynamic environment with opportunities for development and growth, where people are our greatest asset.
**We are Top Employers**
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**We are \#TopEmployers2026 in Spain!** This Top Employers Spain certification recognizes our commitment to employee well-being, as well as our policies and procedures for caring for each individual who is part of Sanitas. And most importantly, **it drives us to keep improving!**