Senior Clinical Data Scientist

2 weeks ago

bareilly, India beBeeStatistical Full time

Statistical Programming LeadThis role requires a skilled professional to oversee the implementation of reporting and analysis activities for clinical trials, generate datasets, complex listings, tables, and graphs using SAS and R programming languages.The ideal candidate will have extensive experience in CDISC standards, medical terminology, and FDA/ICH regulations.Key Responsibilities:SAS Development: Develop high-quality statistical programming results, including developing, validating, and maintaining SAS programs tailored to clinical development programs' needs.Study Oversight: Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet pre-specified timelines.About This Opportunity:We are seeking an experienced Statistical Programmer to join our team. As a key member of our clinical development group, you will be responsible for implementing reporting and analysis activities for clinical trials.Requirements:Master's degree in Biostatistics, Statistics or related field.Possess excellent analytical and problem-solving skills.Demonstrate expertise in CDISC standards, medical terminology, and FDA/ICH regulations.Show strong leadership skills and communication abilities.

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