Statistical Programmer
2 weeks ago
Job Title: Statistical ProgrammerLocation: PAN IndiaExperience: 3 - 12 yearsIndustry: Pharmaceuticals / Biotechnology / Clinical ResearchAbout the RoleWe are looking for an experienced Lead Statistical Programmer to oversee programming activities for clinical trials, regulatory submissions, and integrated analyses. This role involves leading a team, ensuring high-quality deliverables, and developing efficient programming standards to support drug development.Key ResponsibilitiesLead statistical programming activities for a compound or therapeutic area.Manage, mentor, and guide a team of statistical programmers.Create and validate analysis data sets (ADaM), tables, listings, and figures (TFLs) following CDISC standards.Develop and validate Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) reports.Ensure accuracy and consistency across clinical studies and integrated data.Develop, test, and implement reusable standard programs and SAS macros to automate routine tasks.Prepare reviewer guides, data definition documents, and other materials for regulatory filings.Collaborate with cross-functional teams including Statisticians, Clinical Data Management, Medical Writing, Regulatory, and Clinical Operations.Accurately estimate programming efforts and ensure timely project delivery.Required SkillsStrong proficiency in SAS programming; experience with R preferred.In-depth knowledge of CDISC standards (ADaM, SDTM).Experience with regulatory submissions (FDA, EMA) and clinical study lifecycle.Knowledge of therapeutic areas such as Oncology, Immunology, Neuroscience.Strong communication and leadership skills to guide teams and manage stakeholders.Ability to handle multiple priorities and deliver high-quality results under deadlines.Why Join Us?Work on cutting-edge clinical trials and regulatory submissions.Collaborate with a team of top-tier professionals.Opportunity to develop advanced programming frameworks and drive innovation in data analytics.
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Lead Statistical Programmer
2 weeks ago
solapur, India beBeeProgramming Full timeJob SummaryWe are seeking a skilled Statistical Programmer Lead to oversee programming activities for multiple studies/projects in various therapeutic areas.Lead statistical programming initiatives to ensure timely and high-quality deliverables in assigned projects.Develop and maintain programming standards, create CDISC standard SDTM mapping specifications,...
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Advanced Statistical Programmer
2 weeks ago
solapur, India beBeeProgramming Full timeStatistical Programmer RoleWe are seeking skilled Statistical Programmers with CDISC knowledge and R programming expertise to work in a statistical and programming team, providing programming support to various clients.We offer a high-quality statistics consultancy for clients and an industry-leading working environment with support and training for career...
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Statistical Programming Lead
2 weeks ago
solapur, India beBeeData Analyst Full timeJob SummaryThe Senior Statistical Programmer will play a pivotal role in supporting end-to-end clinical programming activities across multiple studies. This position requires strong technical proficiency, autonomy, and collaboration within cross-functional teams.Develop, validate, and maintain clinical trial datasets and outputs using advanced statistical...
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Data-Driven Statistical Expert
1 week ago
solapur, India beBeeProgrammer Full timeStatistical Programmer Job DescriptionThis role entails various responsibilities, including programming support for clients in a portfolio.You will develop dataset specifications and attend study team meetings to ensure effective collaboration and knowledge sharing within the team.Daily interactions include communication with study team members and client...
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Data Analyst and Statistician
2 weeks ago
solapur, India beBeeStatistical Full timeSenior Statistical ProgrammerWe are seeking a highly skilled Senior Statistical Programmer to join our team. As a Senior Statistical Programmer, you will play a key role in the development and implementation of statistical analysis plans for clinical trials.Required Skills and Qualifications:Strong SDTM expertiseOncology study experienceProficient in SAS and...
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Advanced Data Analyst and Statistician
3 days ago
solapur, India beBeeStatistical Full timeJob Summary: We are seeking a Senior Statistical Programmer to lead our data analytics initiatives.As a Senior Statistical Programmer, you will be responsible for generating summary tables, data listings, graphs and derived datasets using advanced statistical techniques and software tools.You will work closely with our team to ensure that outputs meet high...
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Data Analyst and Biostatistician
2 weeks ago
solapur, India beBeeStatistical Full timeSenior Statistical Programmer Job OverviewThis is a sponsor-dedicated role where you will work fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you.As a senior statistical programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or...
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Senior Data Analyst
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solapur, India beBeeStatistical Full timeKey Roles and ResponsibilitiesSponsor-dedicated: Working fully embedded within a pharmaceutical client, you'll be at the heart of their innovation.As a Principal Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work...
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Lead Software Developer
1 week ago
solapur, India beBeeProgramming Full timeJob DescriptionAs a Senior/Principal Programmer, you will be responsible for providing programming support to our statistics and programming department across various projects, clients, and therapeutic areas.This role requires expertise in manipulating large databases, generating reports, and enabling analysts to explore real-world healthcare data...
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Clinical Programming Expert
5 days ago
solapur, India beBeeProgramming Full timeStatistical Programmer LeadJob Overview: Leverage programming expertise to drive clinical studies and projects forward.Independently implement and execute programming standards to support ongoing clinical studies, study reports, regulatory submissions, and ad hoc/post hoc analysis.Collaborate with internal stakeholders and external service providers to...