Clinical Data Processor, Specialty Solutions

🕒 December 16, 2025

🇮🇳 India – Remote

⏰ Full Time

🟢 Junior

⬇️ Data Entry

🚫👨‍🎓 No degree required

👻 Ghost score 65%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Open for 329 days.
• Jobs at this company usually fill in 27 days.
• Reposted 2 times.
• No salary listed.

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Clario

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1973

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 Private Equity Round on 2019-10

Healthcare • Consulting • Logistics

Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

📋 Description

• 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

🎯 Requirements

• 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

🏖️ Benefits

• Competitive pay • Shift allowances and incentives • Provident fund • Medical insurance • Engaging employee programs and local events • Modern office spaces • Remote work flexibility

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