Company OverviewTango Therapeutics is a clinical-stage biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.Tango's labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts.SummaryTango has an exciting opportunity to join our growing Biostatistics team as an Associate Director, Statistical Programming, reporting to the Senior Director of Statistical Programming. In this role, you will be responsible for study-specific statistical programming activities, maintaining programming infrastructure, and ensuring compliance with SOPs to deliver high-quality, timely outputs.Your RoleLead and manage the statistical programming activities for clinical trials and studies, ensuring high-quality and timely deliverables for CSR, publications, presentations, various reports for health authority submissions, clinical data review, and ad hoc analysis either internally or through CRO partnersDevelop, validate, and maintain analysis datasets (SDTM, ADaM), tables, listings, and figures, TLFs) in accordance with regulatory guidelines and internal standardsReview key clinical study or program documentsPerform complex statistical analyses and simulations using SAS to support clinical trial design and data interpretation; manage macro library and templates for efficiently preparing, processing, analyzing clinical data and validating analysis resultsProvide expertise in statistical programming for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD)Participate in Tango’s Data Governance Team to build and maintain secure statistical computing and programming infrastructureCollaborate with biostatisticians, data managers, and cross-functional team members to define programming strategies and requirements, establish project timelines, and perform statistical analysesManage and provide oversight of CROs to ensure high-quality statistical analysis deliverables (datasets, TLFs, etc.) within timeline and budgetAuthor or Review SDTM and ADaM specifications to ensure compliance to CDISC standardsReview key clinical study or program documentsDevelop SAS code, manage macro library and templates for efficiently preparing, processing, analyzing clinical data, and validating analysis resultsAuthor and/or review statistical analysis related SOPsStay current with industry trends, best practices, and emerging technologies in statistical programming and data analysisAdditional duties and responsibilities as requiredWhat You BringBachelor’s or Master’s degree in statistics, life sciences, computer science, or related field with at least 8 years’ statistical programming experienceSolid understanding of industry standards applicable to clinical study data and regulatory reporting requirements including eCTD and CDISC implementationExpert level expertise in SAS programming (Base, Macro, STAT, GRAPH, SQL) is essential; with experience delivering complex programming assignments, macros, and analysesExperience with R and PythonExtensive experience in early-phase clinical studies including programming and validation of SDTM and ADaM data sets, tables, listings and figuresExperience managing CROs for outsourced statistical programming activitiesExpertise in the requirements and technology to support electronic submissionsExperience in oncology preferredExperience with BLA or NDA/sNDA submissions to FDA/EMA requiredStrong analytical and communication skillsWe are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.Salary range $172,000—$258,000 USD
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