Vor Bio
Associate Director, Statistical Programmer
Join Us in Tackling Autoimmune Disease at Its Root Vor believes science can change the course of disease by advancing telitacicept, a first- and potentially best-in-class dual BAFF/APRIL inhibitor, and by addressing disease at its root. You will be part of a mission to redefine the future of autoimmune care. Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases. Growth: Be part of a rapidly scaling company with opportunities to grow your career in science, clinical development, commercial strategy, and beyond. Innovation: Work on a platform with potential beyond one indication with proven results across lupus, IgA nephropathy, and Sjögren’s syndrome. Belonging: Join a culture where every voice is heard and the mission unites us across functions and geographies. Responsibilities
Responsible for performing data and statistical analysis in multiple clinical studies and collaborating with study statisticians, data managers, and other functions on the clinical study team. Provide technical guidance on clinical project teams and participate in design, development, and quality control for SAS programs used to access, extract, transform, review, analyze, and submit clinical data for individual studies. Participate in departmental and cross-functional technology development and process improvement initiatives. Lead study programming activities including review of SAP, setting up mock TFLs, dry runs, and drafting and finalizing TFLs. Collaborate with other functions for requirements (e.g., safety updates, publications). Design and develop SAS programs including macros for efficiency and consistency; contribute to standardization and process improvements. Support FDA submissions as needed. Code complex SAS programs (Macro language, SAS/STAT, SAS/GRAPH) for analysis and reporting of complex clinical trial data and submission of data in CDISC SDTM/ADaM formats. Perform quality control checks of SAS code and outputs; demonstrate proficiency in clinical development and medical data. Resolve clinical trial reporting problems and support daily operations with limited supervision. Create CDISC datasets by transforming raw data from various EDC databases and IWRS and prepare tables, figures, and listings for regulatory submissions. Work with coding dictionaries (MedDRA, WHODD) used in the pharmaceutical industry. Provide technical leadership in a team environment, ensuring quality within budget and timelines. Qualifications
Master’s degree in Statistics, Mathematics, Computer Science, or equivalent. Minimum 8 years of SAS programming experience in pharmaceutical, biotech, or CRO settings. Strong knowledge of CDISC standards (SDTM, ADaM, metadata, controlled terminologies) and data submission processes to FDA. Hands-on SAS programming skills with experience in clinical trial reporting. Ability to manage multiple development programs simultaneously and adapt to changing organizational needs. Strong interpersonal and written/oral communication skills. Benefits
Vor supports its team with robust benefits, including comprehensive health coverage, flexible paid time off, generous parental leave, and a competitive 401(k). We invest in well-being through education assistance, wellness resources, and financial security. Equal Opportunity
As an equal opportunity employer, Vor Bio does not discriminate on the basis of race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. We welcome diverse candidates and believe diversity inspires innovation, inclusiveness, and creativity.
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Join Us in Tackling Autoimmune Disease at Its Root Vor believes science can change the course of disease by advancing telitacicept, a first- and potentially best-in-class dual BAFF/APRIL inhibitor, and by addressing disease at its root. You will be part of a mission to redefine the future of autoimmune care. Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases. Growth: Be part of a rapidly scaling company with opportunities to grow your career in science, clinical development, commercial strategy, and beyond. Innovation: Work on a platform with potential beyond one indication with proven results across lupus, IgA nephropathy, and Sjögren’s syndrome. Belonging: Join a culture where every voice is heard and the mission unites us across functions and geographies. Responsibilities
Responsible for performing data and statistical analysis in multiple clinical studies and collaborating with study statisticians, data managers, and other functions on the clinical study team. Provide technical guidance on clinical project teams and participate in design, development, and quality control for SAS programs used to access, extract, transform, review, analyze, and submit clinical data for individual studies. Participate in departmental and cross-functional technology development and process improvement initiatives. Lead study programming activities including review of SAP, setting up mock TFLs, dry runs, and drafting and finalizing TFLs. Collaborate with other functions for requirements (e.g., safety updates, publications). Design and develop SAS programs including macros for efficiency and consistency; contribute to standardization and process improvements. Support FDA submissions as needed. Code complex SAS programs (Macro language, SAS/STAT, SAS/GRAPH) for analysis and reporting of complex clinical trial data and submission of data in CDISC SDTM/ADaM formats. Perform quality control checks of SAS code and outputs; demonstrate proficiency in clinical development and medical data. Resolve clinical trial reporting problems and support daily operations with limited supervision. Create CDISC datasets by transforming raw data from various EDC databases and IWRS and prepare tables, figures, and listings for regulatory submissions. Work with coding dictionaries (MedDRA, WHODD) used in the pharmaceutical industry. Provide technical leadership in a team environment, ensuring quality within budget and timelines. Qualifications
Master’s degree in Statistics, Mathematics, Computer Science, or equivalent. Minimum 8 years of SAS programming experience in pharmaceutical, biotech, or CRO settings. Strong knowledge of CDISC standards (SDTM, ADaM, metadata, controlled terminologies) and data submission processes to FDA. Hands-on SAS programming skills with experience in clinical trial reporting. Ability to manage multiple development programs simultaneously and adapt to changing organizational needs. Strong interpersonal and written/oral communication skills. Benefits
Vor supports its team with robust benefits, including comprehensive health coverage, flexible paid time off, generous parental leave, and a competitive 401(k). We invest in well-being through education assistance, wellness resources, and financial security. Equal Opportunity
As an equal opportunity employer, Vor Bio does not discriminate on the basis of race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. We welcome diverse candidates and believe diversity inspires innovation, inclusiveness, and creativity.
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