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 Germany.
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.
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.
Requirements
- 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.
Benefits
- Permanent, full-time position with flexible working arrangements (remote within Europe or hybrid in Antwerp).
- Competitive salary and comprehensive benefits package.
- 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.
- Clear career growth opportunities within a rapidly expanding organization.
- Exposure to international clinical research projects and multidisciplinary teams.
- Collaborative and supportive work environment with highly skilled professionals.
- Chance to contribute to meaningful scientific work that impacts healthcare and patient therapy worldwide.
How Jobgether works
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
Data Privacy Notice
By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
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