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Data Curation SME
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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 (OncoLLM) 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 and developing Oncology Data dictionaries, liquid tumor pipeline from scratch and SOP creation by acting as an SME for the liquid tumor portfolio, along with secondary duties of Curation/Abstraction etc.
Position Summary:We are seeking a highly skilled and experienced Data Curation Subject Matter Expert (SME) in Liquid Cancers to join our Oncology Clinical Team. This role will focus on the review of clinical data specifically related to hematologic malignancies (e.g., leukemia, lymphoma, myeloma), and contribution to the development of data dictionaries, SOPs, and AI training pipelines to support oncology trials. Abstraction and curation may also be required based on project requirements.
Essential Job Functions:Serve as the oncology data curation SME for various liquid tumor types. Develop and maintain liquid tumor data libraries; coordinate with cross-functional teams to meet project-specific requirements - from a data curation/RWE perspective. Contribute proactively to pipeline optimization for liquid tumors.
Apply critical thinking to identify, troubleshoot, and escalate issues during data pipeline operations. Proactively contribute to streamlining processes specifically to the liquid tumor pipeline. Ability and flexibility to render support to other projects when there is a team requirement.
Conduct additional duties as assigned, including review of selected medical records to assess eligibility for new project, performing second level reviews/QC review of medical records. Screening of cases for relevant clinical trials across various projects and/or disease subtypes. Knowledge related to cancer trials is essential and required, including understanding their inclusion and exclusion criteria.
Respond promptly to queries issued by the Lead Data Abstractor, Operations Manager or other project personnel. Access electronic data systems for review of medical records and enter specific data into congruent electronic data systems. Ability to understand the Inclusion, Exclusion criteria, adverse event, hospitalization data, medications details and categorize the data accordingly.
Review project specific documents, as needed, to develop familiarity with project goals and with the Abstractor tasks in each project. Ability to understand the diagnostic, pathology and other reports and obtain the exact information required according to trial specific SOPs. Use other resources as needed to gain the knowledge required to perform Abstractor work on new projects.
Share medical knowledge and project-specific procedural knowledge with other Data Abstractors as needed. Qualification:Minimum 4-5 years experience across data abstraction/curation, with a strong focus on liquid tumors and/or expertise is essential - Previous experience in a data curation SME role is desirable. In depth knowledge across the liquid tumor domain with a solid understanding of foundational liquid tumor concepts is also essential.
Oncology experience is preferable; familiarity with how cancer is treated from diagnosis through treatment and recovery and an understanding of cancer terminology is essential. Experience in clinical research or related fields, especially in oncology trials is preferred. An advanced level of clinical knowledge associated with chronic disease states is required.
Experience in clinical research or reviewed medical data for clinical trials. Certification done in clinical research or clinical data management. Education: B.Sc (Nursing), BDS, BAMS, BHMS, MDS, BPharm, MPharm Skills and Abilities:Flexibility: Flexibility in coping with changing work assignments, changing project requirements, varying training meeting schedules, and database resources that may not always function optimally.
Innovation and Proactiveness: Should be able to foresee the probable functionalities and/or think out of the box as complex problems may sometimes require innovative solutions. Language: Strong communication skills both written and verbal to work with multiple internal and external clients in a fast paced environment. Reasoning: Ability to make independent judgments in abstracting medical data and the knowledge of when to seek input from other staff.
Computer: Ability to create and maintain documents using Microsoft office( word, excel, outlook and powerpoint)Why Join US ? 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. We have had company - sponsored workations in Bali, Sri Lanka, and Manali and take pride in our hard-working yet super fun culture .
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. You will get a chance to work with experts from multiple industries and the best in the industry compensation.
