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Urgent! ProcDNA - Senior Statistical Programmer - R/SAS Job Opening In Pune – Now Hiring PROCDNA ANALYTICS PRIVATE LIMITED

ProcDNA Senior Statistical Programmer R/SAS



Job description

<p><p><b>Position :</b> Senior Statistical Programmer<br/><br/><b>Experience :</b> 6+ Years<br/><br/><b>Job Type :</b> Full-time<br/><br/><b>Key Responsibilities :</b><br/><br/></p><p>- Leverage advanced proficiency in SAS and R programming to support or lead complex clinical studies, ensuring data integrity and quality.<br/><br/></p><p>- Perform hands-on programming activities, including the creation of SDTM and ADaM datasets, as well as the generation of Tables, Listings, and Figures (TLFs) for both safety and efficacy analysis.<br/><br/></p><p>- Take ownership of programming tasks with minimal supervision, demonstrating a deep understanding of the study's statistical analysis plan and data structures.<br/><br/></p><p>- Lead all aspects of a clinical study under supervision, including coordination with data management, biostatistics, and clinical teams.<br/><br/></p><p>- Create and maintain comprehensive documentation, including CRF annotations, dataset specifications (SDTM, ADaM, SDRG), and a define.xml for submission.<br/><br/></p><p>- Identify gaps in current programming best practices and propose suggestions for improvement to enhance efficiency and compliance.<br/><br/></p><p>- Ensure strict adherence to applicable policies, procedures, and evolving industry standards.<br/><br/></p><p>- Take responsibility for the timely and accurate completion of all assigned development tasks, from initial programming to final submission.<br/><br/><b>Required Skills & Qualifications :</b><br/><br/></p><p>- 6+ years of hands-on experience in SAS and R programming within a clinical trial environment.<br/><br/></p><p>- Proven proficiency in CDISC standards, with practical experience in creating SDTM and ADaM datasets.<br/><br/></p><p>- Hands-on experience with the generation of TLFs for both safety and efficacy analysis.<br/><br/></p><p>- Experience with CRF annotations and the creation of dataset specifications.<br/><br/></p><p>- Demonstrated ability to lead at least one clinical study under supervision.<br/><br/></p><p>- A strong understanding of the clinical trial domain and the ability to apply this knowledge to programming activities.<br/><br/></p><p>- The ability to execute a wide range of programming activities with minimal supervision.<br/><br/><b>Preferred Skills :</b><br/><br/></p><p>- Experience with electronic submission processes (define.xml, P21, ADRG, SDRG).<br/><br/></p><p>- Familiarity with other programming languages, such as Python, for data analysis.<br/><br/></p><p>- Experience with SAS Grid or other high-performance computing environments.<br/><br/></p><p>- Knowledge of statistical methodologies used in clinical trials.<br/><br/></p><p>- Strong communication skills and the ability to work effectively in a team-based environment.</p><br/></p> (ref:hirist.tech)


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Mathematical Science Occupations



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