Senior Medical Data Abstractor

About Triomics :

Triomics is building the modern technology stack for oncology trial sites and investigators that unifies the workflows of clinical care and clinical research, moving the healthcare industry closer to the vision of Clinical Research as a Care Option. Our platform, which is based on our proprietary oncology-focused large language model (OncoLLMTM) co-developed with several leading cancer centers, eliminates the operational inefficiencies in patient recruitment, data curation, and other laborious tasks involved in clinical research, thus enabling the generation of high-quality data and speeding up the clinical trials.

Job Description :

Part of the Oncology Clinical Team, working on building Oncology Data dictionaries, Curation / Abstraction, SOPs, clinical trial - study build, etc.

Position Summary :

The Person navigates electronic medical record systems and other medical databases. This role involves reviewing clinical trial data for consistency, completeness, and compliance with study protocols and regulatory requirements. reviews medical records, and abstracts medical record data related to specified disease and project requirements.

Essential Job Functions :

• Screen patient cases for eligibility across multiple oncology clinical trials, applying trial-specific inclusion / exclusion criteria.
• Interpret diagnostic, pathology, imaging, and other clinical reports to extract accurate, trial-relevant information per SOPs.
• Abstract and categorize clinical data (e.g., adverse events, hospitalizations, medications) and enter it into designated electronic systems with high accuracy.
• Serve as an oncology subject-matter expert across solid and hematologic malignancies; maintain up-to-date knowledge of cancer trial designs and requirements.
• Apply critical thinking to understand complex clinical concepts and make sound, documented abstraction decisions.
• Build and maintain data libraries; coordinate with cross-functional teams to address project-specific needs.
• Review project documentation to align with goals, timelines, and abstraction workflows; leverage approved resources to onboard quickly to new projects.
• Share medical and procedural knowledge with peers; provide guidance to Data Abstractors as needed.
• Respond promptly to queries from Leads / Operations and collaborate to resolve data issues.
• Perform additional tasks as assigned, including preliminary eligibility reviews and second-level / QC reviews of medical records.

Qualification :

Education :

B.Sc (Nursing), BDS, BAMS, BHMS, MDS, BPharm, MPharm

Skills and Abilities :

Why Join us ?

1. We are revolutionizing a unique industry that has the potential to impact and benefit patients

from all over the world - you can create impact at scale.

2. We have had company - sponsored workations in Bali, Sri Lanka, and Manali and take pride in our hard-working yet super fun culture .

3. We are working on a few of the most challenging problems in a highly regulated industry which provides you an opportunity to solve some of the most interesting things.

4. You will get a chance to work with experts from multiple industries and the best in the industry

Compensation.

Please Brush your knowledge / Skills on below areas and also Glance through your resume for the discussions :