Our partner is looking for a Data Manager based in Spain.

In this role, you will be responsible for ensuring the accuracy, consistency, and integrity of critical clinical trial data that supports advancements in life sciences and patient care. You will work at the intersection of data management, clinical research, and technology, contributing to high-quality data processes that directly impact scientific outcomes. This position offers the opportunity to collaborate closely with clinical project teams and external partners while managing the full lifecycle of clinical data systems. You will design, validate, and optimize databases and data transfer processes in a highly regulated environment. The role is ideal for detail-oriented professionals who enjoy working with complex datasets and thrive in structured, quality-driven environments. Oversee data management activities for clinical trials, ensuring accuracy, integrity, and consistency of all study-related data.

Collaborate closely with clinical project managers to align data management processes with study requirements and timelines.

Design, develop, validate, and maintain project-specific clinical databases.

Define and implement data transfer specifications in coordination with internal teams and external clients.

Program, validate, and execute data exports using tools such as SQL and R.

Ensure high-quality and timely delivery of all data transfers and reporting outputs.

Support continuous improvement of data workflows, standards, and documentation practices.





Bachelor's or Master's degree in a scientific field such as biomedical science, biology, pharmaceuticals, medicine, bioinformatics, or equivalent experience in data management.

Proven experience in data management, preferably within a pharmaceutical, biotech, or clinical research environment.

Strong proficiency in SQL and experience working with structured databases.

High attention to detail with a strong focus on data accuracy and quality assurance.

Affinity for IT systems and data-driven workflows.

Familiarity with regulated environments such as CAP, CLIA, or GCP, as well as FDA-related guidelines, is a plus but not required.

Permanent, full-time position with versátil working arrangements (remote within Europe or hybrid in Antwerp).

Opportunity to work in a global, science-driven environment focused on improving patient outcomes.

Strong emphasis on training, learning, and professional development across technical and soft skills.

Exposure to international clinical research projects and multidisciplinary teams.

Collaborative and supportive work environment with highly skilled professionals.

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📌 Chief Data Officer (Remote) (Málaga)
🏢 Jobgether
📍 Málaga