Our mission is to improve health equity by expanding access to cancer precision medicine. Trial Library, Inc. is a venture-backed startup founded in 2022 to address inequities in clinical trial participation. Our technology is integrated with human-led navigation to enable clinical trial discovery for anyone, anywhere. Our vision is to be the leading discovery and recruitment platform for inclusive clinical trials. We are a diverse team of experts who believe that health equity starts with patient and provider empowerment. We believe that inequities in clinical trial access need to be addressed creatively and intentionally. We believe that inclusive research environments can answer questions that improve health outcomes for all , not just the few who participate in clinical trials. We believe in the power of technology to disseminate high quality health information about clinical trials sustainably. We believe in the power of representation in online health communication. The Data Analyst at Trial Library will play an integral part in expanding access to cancer clinical trials by supporting the development of a clinical trial matching tool and pioneering pre-screening efforts in community oncology settings. You will work closely with the Product and Operations teams at Trial Library. You will be responsible for translating complex clinical trial protocols into structured, standardized data that supports the matching of patients to appropriate clinical trials. Your work will involve close collaboration with clinical staff, stakeholders, and project teams to ensure that data collection processes are streamlined and optimized for accuracy and efficiency. This role requires strong attention to detail, analytical skills, and a deep understanding of clinical trials. Your Responsibilities Review and abstract clinical data from various sources including electronic and paper medical records, various databases, and clinicaltrials.gov Use predefined SOPs to capture key data elements and ensure consistency in data collection Apply quality control procedures to identify and resolve data inconsistencies, discrepancies, or missing information in the abstraction process Collaborate with internal stakeholders and Subject Matter Experts to refine data collection processes to streamline the capture of clinical trial data Use reference material to appropriately facilitate accuracy and completeness of reports Prepare pre-screening charts for clinician review and maintain source documentation Compile daily and weekly pre-screening reports for Trial Library leadership Document and maintain technically accurate best practices in SOPs for medical chart abstraction, reporting, and other data-related activities Serve as liaison and resource for community oncology practices Follow established policies and procedures to protect the confidential nature of clinical data Be willing to travel to clinics, up to 25% of time Your Qualifications Prior direct experience with clinical data abstraction and a minimum of 2 years working in a clinical research setting with site level experience supporting clinical trial operations, with a focus on oncology preferred Working knowledge of medical terminology required Demonstrated proficiency in multiple software systems and EMRs used in hospital and clinical settings such as Epic Systems Corporation, Oracle Cerner, OncoEMR (Flatiron), Aria Oncology Information System (Varian), MOSAIQ (Elekta), iKnowMedGeneration 2 (McKesson), etc. Prior experience using Excel, Google Suite, Qualtrics, SQL, Tableau Strong ability to multitask and complete a high volume of work within deadlines Exceptional attention to detail and strong organizational skills Familiarity with publicly available clinical trial databases such as clinicaltrials.gov Experience in data entry, data cleaning & management, and data quality assurance Excellent communication skills to collaborate with clinical and non-clinical stakeholders Bachelor’s or equivalent degree required Our Core Values
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