• develop predictive models, risk and profitability logic, and scenario/forecast frameworks that translate claims, contract terms, and market signals into the numbers our deal teams act on • partner with underwriters, pricing actuaries, and finance to translate business questions into testable code — pricing calculators, P&L tools, recurring forecasts, and the rule engines underneath them • balance a long-running model build, a quick-turn analysis for a sales leader, and a recurring reporting cycle in the same week

• Provide on-field support for pre-and post-sales activities with direct customers and channel partners • Educate, train, and support new and existing customers on Lunaphore instrumentation and data analysis solutions • Collaborate with account managers to expand instrument, software, and consumable sales • Attend scientific meetings, conferences, and trade shows to present company products, applications, and data • Investigate issues relating to hardware, software, and biological assays and develop solutions to address them • Report and present feedback from the field through thorough and detailed presentations • Develop multiplex staining assays and evaluate stained tissues

• Author and coordinate development of clinical pharmacology trial protocols and ensure timely review, approval, and issuance • Perform preliminary, interim, and final PK, PD, and PK/PD analyses using non-compartmental methods • Develop the Clinical Pharmacology Analysis Plan (CPAP) and generate data handling logbooks prior to final NCA • Create tables, listings, and figures and contribute to drafting clinical pharmacology sections of Clinical Study Reports (CSRs) • Conduct QC review of protocols, analyses, datasets, and all deliverables while ensuring compliance with SOPs, ICH-GCP, and regulatory requirements

• Data analysis and interpretation • Perform PK analyses independently • Assist with PD analyses • Interpret PK and statistical results and findings independently • Perform QC reviews as assigned • Write and review reports as assigned • Prepare PK data/report files for electronic filing of projects for submission to regulatory agencies • Maintain and file all supportive documentation pertaining to the study and ensure proper archiving of projects • Other responsibilities • Interact with clients alongside or under direction of a senior scientist, as needed • Prepare internal presentations