Roles & Responsibilities
• Manage end-to-end Clinical Data Management deliverables for assigned clinical studies
• Review and evaluate clinical data generated from imaging components of sponsor trials
• Participate in client and project meetings as required
• Understand study requirements for data collection and implementation
• Collaborate with project teams to develop study-specific edit check criteria
• Define, execute, and review edit checks; resolve discrepant data
• Perform study setup including database structure, specifications, and TF design
• Coordinate receipt and processing of electronic and ancillary data from external sources
• Review clinical data for errors and inconsistencies and drive resolution
• Track outstanding data issues and ensure timely closure
• Maintain complete, accurate, and audit-ready study documentation
• Ensure all CDM activities comply with SOPs, regulatory guidelines, and quality standards
• Support SOP updates and contribute to continuous process improvement
• Maintain technical and industry knowledge through ongoing training
Qualification
• Bachelor’s degree in Computer Science, Life Sciences, or a related field
• Equivalent professional experience may be considered
Experience
• Minimum 1 year of experience in Clinical Data Management
• Experience in pharma, biotech, or CRO environment preferred
Skills
• Strong knowledge of Clinical Data Management processes
• Understanding of relational database structures and data validation
• Familiarity with SAS is desirable
• Proficiency in MS Word, Excel, and Access
• Knowledge of clinical trial terminology
• Excellent attention to detail and problem-solving abilities
• Strong communication, documentation, and organizational skills
• Ability to work independently and collaboratively in a dynamic environment
About the Organisation
Clario is a global leader in clinical trial endpoint technology, dedicated to transforming evidence generation and improving patient outcomes. The company supports life-changing therapies through innovation, data excellence, and a purpose-driven culture, offering flexible work options, competitive benefits, and opportunities to make a meaningful impact in global clinical research.
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