Clinical Data Processor, Specialty Solutions

• Execute study-specific workflows including creation, resumption, cancellation, and completion of Workflow Runs
• Review and redact images, videos, and documents per study parameters and timelines
• Provision customer user accounts for assigned studies and trials
• Facilitate source document translation and create DICOM image links as needed
• Use tools such as SightHound and PDF redaction software to process source documents
• Issue queries and follow up with study sites to resolve documentation issues
• Support generation and distribution of final study closeout deliverables
• Collaborate with cross-functional teams to ensure proper tool usage and adherence to specifications
• Attend project and team meetings to align on study progress and expectations
• Maintain high standards of quality, professionalism, and accountability in all deliverables

What We Look For

• High school diploma or Associate/Bachelor’s degree in computer science, information technology, or related field
• 10months–1 year of experience in clinical trials, healthcare, or a related domain; 1+ year preferred
• Proven expertise in MS Office tools including Word, Excel, Teams, and OneNote
• Strong proficiency in identifying PII/PHI and applying Good Documentation Practices
• Demonstrated ability to work independently and collaboratively in dynamic environments
• Fluency in English (written and verbal)
• Willingness to work European or US time zone shifts
• 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.