Clinical Data Processor – Specialty Solutions | Full-Time | Bangalore, India / Remote
Category: Clinical Data / Specialty Solutions | Location: Bangalore, India (Remote Eligible)
Company: Clario
Company Overview:
Clario is a global leader in clinical research solutions, supporting pharmaceutical and biotech companies in delivering safe and effective therapies to patients worldwide. Our Specialty Solutions team ensures high-quality data management and process excellence across complex clinical trials, enabling faster and more reliable evidence generation.
Position Overview:
Clario is seeking a Clinical Data Processor to join our Specialty Solutions team. In this role, you will ensure the accuracy, compliance, and integrity of clinical trial documentation, supporting the delivery of life-changing therapies. The ideal candidate is detail-oriented, tech-savvy, and committed to maintaining high standards of quality and regulatory compliance.
Key Responsibilities:
Execute study-specific workflows, including creation, resumption, cancellation, and completion of Workflow Runs.
Review, redact, and process images, videos, and documents according to study parameters and timelines.
Provision and manage customer user accounts for assigned studies and trials.
Facilitate source document translation and create DICOM image links as required.
Utilize tools such as SightHound and PDF redaction software to process source documents accurately.
Issue queries and liaise with study sites to resolve documentation issues promptly.
Support generation and distribution of final study closeout deliverables.
Collaborate with cross-functional teams to ensure proper tool usage and adherence to study specifications.
Attend project and team meetings to align on study progress and expectations.
Maintain professionalism, accountability, and quality standards in all deliverables.
Qualifications and Experience:
Education:
High school diploma or Associate/Bachelor’s degree in Computer Science, Information Technology, Life Sciences, or related field.
Experience:
0–2 years of experience in clinical trials, healthcare, or related domains; 1+ year preferred.
Familiarity with Good Documentation Practices (GDP) and handling sensitive information (PII/PHI).
Proficiency in MS Office tools including Word, Excel, Teams, and OneNote.
Skills:
Strong attention to detail and organizational skills.
Ability to work independently and collaboratively in dynamic environments.
Effective written and verbal communication skills in English.
Flexibility to work European or US time zone shifts.
Why Join Clario:
Clario is committed to transforming lives by enabling better clinical evidence. Our employees are empowered to make meaningful contributions, whether advancing clinical science, developing innovative technology, or supporting global study teams. Competitive compensation, flexible work options, and professional development opportunities make Clario a rewarding workplace for motivated professionals.
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