{"schemaVersion":"jobsearcher.job.v1","id":"40ca59a0bf5dc8039fdbaf85","url":"https://jobsearcher.com/jobs/40ca59a0bf5dc8039fdbaf85","canonicalUrl":"https://jobsearcher.com/jobs/40ca59a0bf5dc8039fdbaf85","title":"Manager, Statistical Programming","description":"PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life’s moments for children and adults living with a rare disease.\n\nAt PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.\n\nVisit our website to learn more about our company and culture!\nSite: www.ptcbio.com\n\nJob Description Summary:\n\nThe Manager, Statistical Programming performs the programming activities for clinical development programs and associated clinical studies either directly or through Contract Research Organization (CRO) oversight. Participates in the development of new and review of existing statistical programming standard operating procedures and processes and biostatistics computing systems implementations and application development as appropriate.\n\nThe incumbent works cross-functionally with internal departments and external resources on statistical programming related issues.\n\nThe Manager, Statistical Programming supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.\n.\nJob Description:\n\nESSENTIAL FUNCTIONS\n\nPrimary duties/responsibilities:\n\nContributes to the statistical programming activities for assigned clinical development studies and programs.\nEnsures timely statistical analyses of clinical data per protocols and Statistical Analysis Plans; either directly or through CRO oversight develops statistical programs and produces programmed outputs used to create integrated scientific reports for clinical trial results.\nParticipates in study team meetings as a representative of the Biostatistics function. Contributes to the identification of statistical issues. May collaborate with other members of the statistical programming team to identify solutions. Acts as a statistical/programming resource to the development teams.\nParticipates in the assessment, selection and evaluation of CROs.\nParticipates in the review of Case Report Forms (CRFs), CRF annotations, Statistical Action Plans, TLGs and TLG shells.\nAs appropriate, interacts with CROs involved in data management/analysis activities to ensure that their statistical analyses and resulting outputs are accurate and consistent with the contractually agreed upon deliverables; works with vendor staff to characterize and resolve issues related to data analysis.\nCreates/Reviews derived dataset specifications and the related analysis datasets.\nMay develop SOPs and training guidelines related to statistical programming.\nPerforms other tasks and assignments as needed and specified by management.\n\nKNOWLEDGE/SKILLS/ABILITIES REQUIRED\n\nMinimum level of education and years of relevant work experience.\n\nBachelor’s degree in a quantitative sciences discipline (e.g., Statistics, Mathematics, Computer Science) and a minimum of 5 years of experience in statistics or statistical programming in a pharmaceutical, biotechnology, CRO or related environment.\n\nSpecial knowledge or skills needed and/or licenses or certificates required.\n\nDemonstrated and applied SAS programming skills (e.g., Base SAS, SAS/Stat, SAS/Graph, SAS macros, ODS) and a good understanding of database systems.\nWorking knowledge of R.\nClinical Data Interchange Standards Consortium (CDISC) experience.\nKnowledge of clinical data analysis and reporting process as it relates to drug development.\nExcellent verbal and written communication and skills.\nAbility to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.\nAnalytical thinker with excellent problem- solving skills and the ability to adapt to changing priorities and deadlines.\nExcellent planning, organization and time management skills including the ability to support and prioritize multiple projects.\n\n*Special knowledge or skills and/or licenses or certificates preferred.\n\nMaster’s degree in a quantitative discipline (e.g., Statistics, Mathematics, Computer Science).\nExperience working with CROs.\nExperience supporting New Drug Applications (NDAs) and Marketing Authorisation Applications (MAAs) submissions.\n\nTravel requirements\n\nUp to 15%\n\nExpected Base Salary Range: $134,000 - $160,000. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity. In addition to base salary, PTC employees are also eligible for short- and long-term incentives. All eligible employees may also enroll in PTC’s medical, dental, vision, and retirement savings plans\n\nEEO Statement:\n\nPTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.\n\nClick here to return to the careers page","company":"Ptc Therapeutics","rawCompany":"ptc therapeutics","city":"Hackettstown","state":"NJ","isRemote":false,"isActive":false,"createdAt":"2026-11-05T09:13:28.478Z","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":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Manager, Statistical Programming","description":"PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life’s moments for children and adults living with a rare disease.\n\nAt PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.\n\nVisit our website to learn more about our company and culture!\nSite: www.ptcbio.com\n\nJob Description Summary:\n\nThe Manager, Statistical Programming performs the programming activities for clinical development programs and associated clinical studies either directly or through Contract Research Organization (CRO) oversight. Participates in the development of new and review of existing statistical programming standard operating procedures and processes and biostatistics computing systems implementations and application development as appropriate.\n\nThe incumbent works cross-functionally with internal departments and external resources on statistical programming related issues.\n\nThe Manager, Statistical Programming supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.\n.\nJob Description:\n\nESSENTIAL FUNCTIONS\n\nPrimary duties/responsibilities:\n\nContributes to the statistical programming activities for assigned clinical development studies and programs.\nEnsures timely statistical analyses of clinical data per protocols and Statistical Analysis Plans; either directly or through CRO oversight develops statistical programs and produces programmed outputs used to create integrated scientific reports for clinical trial results.\nParticipates in study team meetings as a representative of the Biostatistics function. Contributes to the identification of statistical issues. May collaborate with other members of the statistical programming team to identify solutions. Acts as a statistical/programming resource to the development teams.\nParticipates in the assessment, selection and evaluation of CROs.\nParticipates in the review of Case Report Forms (CRFs), CRF annotations, Statistical Action Plans, TLGs and TLG shells.\nAs appropriate, interacts with CROs involved in data management/analysis activities to ensure that their statistical analyses and resulting outputs are accurate and consistent with the contractually agreed upon deliverables; works with vendor staff to characterize and resolve issues related to data analysis.\nCreates/Reviews derived dataset specifications and the related analysis datasets.\nMay develop SOPs and training guidelines related to statistical programming.\nPerforms other tasks and assignments as needed and specified by management.\n\nKNOWLEDGE/SKILLS/ABILITIES REQUIRED\n\nMinimum level of education and years of relevant work experience.\n\nBachelor’s degree in a quantitative sciences discipline (e.g., Statistics, Mathematics, Computer Science) and a minimum of 5 years of experience in statistics or statistical programming in a pharmaceutical, biotechnology, CRO or related environment.\n\nSpecial knowledge or skills needed and/or licenses or certificates required.\n\nDemonstrated and applied SAS programming skills (e.g., Base SAS, SAS/Stat, SAS/Graph, SAS macros, ODS) and a good understanding of database systems.\nWorking knowledge of R.\nClinical Data Interchange Standards Consortium (CDISC) experience.\nKnowledge of clinical data analysis and reporting process as it relates to drug development.\nExcellent verbal and written communication and skills.\nAbility to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.\nAnalytical thinker with excellent problem- solving skills and the ability to adapt to changing priorities and deadlines.\nExcellent planning, organization and time management skills including the ability to support and prioritize multiple projects.\n\n*Special knowledge or skills and/or licenses or certificates preferred.\n\nMaster’s degree in a quantitative discipline (e.g., Statistics, Mathematics, Computer Science).\nExperience working with CROs.\nExperience supporting New Drug Applications (NDAs) and Marketing Authorisation Applications (MAAs) submissions.\n\nTravel requirements\n\nUp to 15%\n\nExpected Base Salary Range: $134,000 - $160,000. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity. In addition to base salary, PTC employees are also eligible for short- and long-term incentives. All eligible employees may also enroll in PTC’s medical, dental, vision, and retirement savings plans\n\nEEO Statement:\n\nPTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.\n\nClick here to return to the careers page","datePosted":"2026-11-05T09:13:28.478Z","dateModified":"2026-11-05T09:13:28.478Z","hiringOrganization":{"@type":"Organization","name":"Ptc Therapeutics","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Hackettstown","addressRegion":"NJ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"40ca59a0bf5dc8039fdbaf85"},"url":"https://jobsearcher.com/jobs/40ca59a0bf5dc8039fdbaf85"}}