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
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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鈥檚 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鈥檚 a cause that unites and inspires us. It鈥檚 why we come to work鈥攁nd 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.
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