Contractor - Medical Data Abstractor

Role Overview: You will be a part of the Oncology Clinical team at Triomics, supporting the development of oncology data dictionaries, data curation/abstraction, SOP adherence, and clinical trial study builds. Your responsibilities will include navigating electronic medical records (EMRs) and other clinical data sources to review and abstract information for consistency, completeness, and compliance with study protocols and regulations. Key Responsibilities: - Screen patient cases for eligibility across multiple oncology clinical trials by applying trial-specific inclusion/exclusion criteria. - Interpret diagnostic, pathology, imaging, and other clinical reports to extract accurate, trial-relevant information following SOPs. - Abstract and categorize clinical data (e.g., adverse events, hospitalizations, medications) with high accuracy into designated electronic systems. - Maintain expertise across solid and hematologic malignancies, staying updated on cancer trial designs and requirements. - Apply critical thinking to understand complex clinical concepts and make well-documented abstraction decisions. - Build and manage data libraries, collaborating with cross-functional teams to address project-specific needs. - Review project documentation, aligning with goals, timelines, and abstraction workflows, and quickly onboard new projects using approved resources. - Share medical and procedural knowledge with peers, providing guidance to Data Abstractors as necessary. - Respond promptly to queries from Leads/Operations and collaborate to resolve data issues. - Perform additional tasks as assigned, including preliminary eligibility assessments and second-level/QC reviews of medical records. Qualifications: - 2+ years of experience in clinical data abstraction or patient treatment-related data work. - Strong clinical knowledge of chronic disease states and medical terminology. - Oncology expertise across the care continuum with deep familiarity in solid and liquid tumors. - Experience in reviewing medical data for clinical research, particularly in oncology trials. Education: - B.Sc (Nursing), BDS, BAMS, BHMS, MDS, BPharm, or MPharm. Skills & Abilities: - Excellent written and verbal communication skills to collaborate in a fast-paced environment. - Sound judgment in abstracting medical data, working independently, and seeking input when necessary. - High adaptability to changing assignments, project requirements, and training schedules. - Proficiency in Microsoft Office tools (Word, Excel, Outlook, PowerPoint) for creating, maintaining, and sharing professional documents and reports.,