{"schemaVersion":"jobsearcher.job.v1","id":"21a340812959d43d0e84df5d","url":"https://jobsearcher.com/jobs/21a340812959d43d0e84df5d","canonicalUrl":"https://jobsearcher.com/jobs/21a340812959d43d0e84df5d","title":"Associate Director, Statistical Programming","description":"Overview\r\nThis role at Celldex Therapeutics is a leadership position focused on overseeing the end-to-end statistical programming lifecycle. It combines technical oversight, project management, and cross-functional collaboration to ensure clinical trial data meets rigorous regulatory standards.\r\nResponsibilities\r\n\r\nLead or Co-ordinate statistical programming activities of all programmers either internally or externally assigned to the study/project work, mentor other programmers in functional expertise and processes. Make statistical programming decisions/recommendations at study or project level.\r\nComply with company, department and industry standards (e.g. CDISC) and processes, responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.\r\nOversee the creation of CDISC compliant submission readiness output including but not limited to datasets (SDTM, ADaM), Tables, Listings and Figures (TFLs) and associated Define packages.\r\nOversee the external programming activities outsourced to CROs to ensure the quality including standard programming practice, validation, and documentation.\r\nBuild and maintain effective working relationships with cross-functional teams both internally and externally, contribute to the status of deliverables and critical programming aspects (timelines, scope, resource plan etc.)\r\nSupport all in-house programming activities, if needed, including but not limited to regulatory filings, adhoc analysis, publication requests etc.\r\n\r\nQualifications\r\n\r\nMS in Statistics or related field\r\n8+ years of SAS programming experience in the biotech/pharma industry\r\nExperience as the lead programmer coordinating programming teams to support multiple regulatory submissions\r\nExperience managing people and projects.\r\nProficiency with SAS Base, Macro, SQL, and Graph; working knowledge of R is a plus.\r\nExperience working with and managing external CROs or FSPs for programming deliverables.\r\nFamiliarity with CDISC (SDTM/ADaM) standards and ability to develop SAS code for datasets and TLFs\r\nExcellent communication skills and ability to work cross-functionally in a lean team environment.\r\n\r\nCompensation\r\nThe expected base salary range for this position is $153,616 to $199,501.We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.\r\nCompensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.","company":"Celldex Therapeutics","rawCompany":"celldex therapeutics","city":"Hampton","state":"NJ","isRemote":false,"isActive":false,"createdAt":"2026-05-02T20:37:02.469Z","occupations":[{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"11-9121.00","title":"Natural Sciences Managers","slug":"natural-sciences-managers"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Associate Director, Statistical Programming","description":"Overview\r\nThis role at Celldex Therapeutics is a leadership position focused on overseeing the end-to-end statistical programming lifecycle. It combines technical oversight, project management, and cross-functional collaboration to ensure clinical trial data meets rigorous regulatory standards.\r\nResponsibilities\r\n\r\nLead or Co-ordinate statistical programming activities of all programmers either internally or externally assigned to the study/project work, mentor other programmers in functional expertise and processes. Make statistical programming decisions/recommendations at study or project level.\r\nComply with company, department and industry standards (e.g. CDISC) and processes, responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.\r\nOversee the creation of CDISC compliant submission readiness output including but not limited to datasets (SDTM, ADaM), Tables, Listings and Figures (TFLs) and associated Define packages.\r\nOversee the external programming activities outsourced to CROs to ensure the quality including standard programming practice, validation, and documentation.\r\nBuild and maintain effective working relationships with cross-functional teams both internally and externally, contribute to the status of deliverables and critical programming aspects (timelines, scope, resource plan etc.)\r\nSupport all in-house programming activities, if needed, including but not limited to regulatory filings, adhoc analysis, publication requests etc.\r\n\r\nQualifications\r\n\r\nMS in Statistics or related field\r\n8+ years of SAS programming experience in the biotech/pharma industry\r\nExperience as the lead programmer coordinating programming teams to support multiple regulatory submissions\r\nExperience managing people and projects.\r\nProficiency with SAS Base, Macro, SQL, and Graph; working knowledge of R is a plus.\r\nExperience working with and managing external CROs or FSPs for programming deliverables.\r\nFamiliarity with CDISC (SDTM/ADaM) standards and ability to develop SAS code for datasets and TLFs\r\nExcellent communication skills and ability to work cross-functionally in a lean team environment.\r\n\r\nCompensation\r\nThe expected base salary range for this position is $153,616 to $199,501.We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.\r\nCompensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.","datePosted":"2026-05-02T20:37:02.469Z","dateModified":"2026-05-02T20:37:02.469Z","hiringOrganization":{"@type":"Organization","name":"Celldex Therapeutics","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Hampton","addressRegion":"NJ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"21a340812959d43d0e84df5d"},"url":"https://jobsearcher.com/jobs/21a340812959d43d0e84df5d"}}