Data Manager

New

Remote within Europe or hybrid in AntwerpFull-TimeMiddle

Salary not disclosed

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Job Details

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.

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.

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