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# Data Manager

- **Company:** ProntoPro
- **Location:** Madrid, Spain
- **Salary:** €40,500.0 - €49,500.0
- **Contract:** Permanent contract
- **Skills:** Big Data, Bioinformatics, Clinical Data Repository, Databases, Data Transmissions, Laboratory Information Management Systems, SQL Databases, Information Technology, Data Analytics, Data Management
- **Published:** September 24, 2026
- **Apply:** https://www.adzuna.es/contact-us.html

## About the Role

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.
Analytical mindset with strong problem-solving and critical thinking abilities.
Ability to work independently while managing multiple priorities in a structured environment.
Strong communication, organizational, and time management skills.
Affinity for IT systems and data-driven workflows.
Experience with R, laboratory information systems (LIS), or similar tools is an advantage.
Familiarity with regulated environments such as CAP, CLIA, or GCP, as well as FDA-related guidelines, is a plus but not required.

## Description

This position is listed on behalf of a partner company, who manages all applications and next steps. 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. Your work will play a key role in supporting clinical research programs that contribute to the development of innovative therapies.
Accountabilities
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.
Maintain compliance with applicable clinical research standards and regulatory expectations.