• Perform end-to-end clinical data management activities for assigned studies
• Review and evaluate clinical trial imaging and clinical data for accuracy and compliance
• Collaborate with project teams to define study-specific edit checks
• Run, review, and resolve data queries and discrepancies
• Support study setup including database structure, specifications, and TF design
• Coordinate receipt, integration, and processing of external and electronic clinical data
• Maintain complete, accurate, and audit-ready study documentation
• Track open data issues and ensure timely resolution
• Ensure CDM activities comply with regulatory guidelines and internal SOPs
• Participate in client meetings and cross-functional discussions
• Continuously enhance technical and industry knowledge through training
• Bachelor’s degree in Life Sciences, Computer Science, or a related discipline
• Equivalent clinical data management experience will be considered
• Minimum 1 year of experience in Clinical Data Management (Pharma, Biotech, or CRO)
• Strong understanding of clinical trial terminology and CDM processes
• Working knowledge of relational databases and data validation
• SAS knowledge is desirable
• Proficiency in MS Word, Excel, and Access
• Strong analytical skills with high attention to detail
• Excellent documentation, organizational, and communication skills
• Ability to work independently and effectively in fast-paced team environments
Clario is a global leader in clinical trial endpoint technology, delivering innovative imaging, cardiac safety, and digital endpoint solutions to support clinical trials worldwide. The company partners with leading pharmaceutical, biotech, and medical device organizations, offering professionals exposure to global studies, advanced technology platforms, and diverse therapeutic areas.
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