Join Clario as a Clinical Data Manager in Hungary (remote) and play a key role in ensuring the quality and integrity of clinical trial imaging data that supports life-changing therapies for patients worldwide.

What we offer

• Competitive compensation

• Attractive benefits (security, flexibility, support and well-being)

• Engaging employee programs

• Remote working and home office allowance

• OTP Szép Card

What you'll be doing

• Review and evaluate clinical data generated from the imaging portion of sponsor clinical trials across various therapeutic areas.

• Perform all data management deliverables for assigned studies, ensuring timelines and quality standards are met.

• Support study setup activities, including eCRF/TF design, database structure, and specifications, obtaining and providing necessary approvals.

• Understand study implementation and data collection requirements and translate these into robust data management plans.

• Collaborate with project teams to develop and maintain study-specific edit check criteria.

• Define, run, and review edit checks, identify discrepant data, and drive timely data query resolution.

• Coordinate, document, and oversee the receipt and processing of electronic or ancillary data from external sources (e.g., central labs, CROs, sponsors).

• Maintain organized, complete, and up-to-date study documentation in accordance with internal and regulatory standards.

• Track outstanding data issues, follow up with stakeholders, and ensure discrepancies are resolved and documented.

• Ensure accuracy and consistency in the manipulation, review, and validation of clinical data, adhering to relevant regulatory guidelines.

• Adhere to Clinical Data Management procedures, policies, and SOPs, and contribute to the review and improvement of departmental standards and processes.

• Collaborate with internal teams to resolve operational issues, share knowledge, and support others in achieving project goals.

• Participate in company-sponsored training to maintain and enhance technical and industry knowledge.

What we look for

• Bachelor’s degree in Computer Science, Life Sciences, or a related field, or equivalent relevant experience.

• Approximately 1+ years of experience in a similar role within the pharmaceutical, biotechnology, or CRO industry.

• Working knowledge of relational database organization and data validation.

• Familiarity with SAS is desirable.

• Experience with office productivity tools such as Word, Excel, and Access.

• Understanding of clinical trial terminology is an advantage.

• Demonstrated problem-solving skills and a proactive, solution-oriented mindset.

• Ability to work independently within a team environment and to adapt to changing priorities.

• Excellent attention to detail with strong documentation and organizational skills.

• Strong interpersonal and communication skills, both verbal and written.

• Ability to project and maintain a professional, positive attitude while working with diverse stakeholders.

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.