Senior SAS Programmer in P-Product, Inc.

P-Product, aleading and innovative company inSoftware development and Data solutions, islooking for anexperienced Senior SAS Programmer tojoin our dynamic team and contribute programming support tothe statistics and programming department across awide range ofprojects, clients, and therapeutic areas. You will have avital role inhelping our clinical trials and drug development processes succeed.Key Responsibilities: •Perform SAS programming tocreate, validate, and maintain analysis datasets, tables, listings and figures for clinical trials and reports according tostudy protocol and statistical analysis plans. •Lead the clinical trials flow development from study protocols development tofinal data analysis, documentation and provisioning the datasets for regulatory submission. •Adhere toGCP, ICH, and other regulatory guidelines for pharmaceutical data reporting, managerial, scientific and technical tasks. •Integrate data from different sources and ensure that the datasets are consistent and reliable. •Collaborate closely with various teams and professionals, such asresearchers, data analysts, biostatisticians, data managers and other key stakeholders, toensure data quality and integrity and observance ofregulatory, industry and company standards. •Coach and mentor junior SAS programmers and create alearning and growth environment.Required Knowledge and Skills: •BSc, MSc orPhD inStatistics, Mathematics, Computer Science, orrelated field. •5+ years ofextensive programming experience inSAS inaclinical trial environment. •Extended experience with SAS/BASE, SAS/MACRO, SAS/GRAPH and SAS/STAT. •Professional knowledge and experience with CDISC clinical data standards, such asCDISC, ADaM and SDTM. •Proven ability todevelop specifications for datasets and outputs ofany complexity according tothe requirements, aswell asindependently write SAS programming code and validation scripts inagood quality manner. •Proven statistical expertise, especially inefficacy outputs programming. •Excellent knowledge ofdrug development processes and regulatory submission requirements. •Exceptional analytical and problem-solving skills, strong organizational and communications skills, high attention todetail and commitment toaccuracy, proactive mindset and capability towork independently aswell asinateam environment.Will BeaPlus: •SAS certification. •Team leading and mentoring experience.