Lead Stat Programmer Clinical Trials

3 days ago

visakhapatnam, India beBeeStatisticalProgramming Full time

Job DescriptionWe are seeking an experienced Statistical Programming Lead to lead one or more Phase I-IV studies programming activities as per the project strategies. This role requires strong SAS programming skills, excellent analytical skills and a good understanding of pharmaceutical clinical development principles.Lead statistical programming activities for multiple studies/projects in various therapeutic areas to ensure timely and high-quality programming deliverables.Develop and maintain programming documentations following programming standards and processes.Create CDISC standard SDTM mapping specifications and ADaM specifications.Key Responsibilities:Develop and oversee the development of SAS programs for the creation of SDTM and ADaM datasets following CDISC standards and reports.Contribute to the development of standard and utility macros and participate in establishing and maintaining statistical programming standards.Participate in the CRF annotation, review of SAP, TLFs specifications development and TLFs review.Required Skills and QualificationsTo succeed in this role, you will need:A minimum Bachelor's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 7-8+ years of programming experience in processing clinical trial data.Strong SAS programming skills and working knowledge of other programming languages such as R, Python etc.Excellent analytical skills and a good understanding of pharmaceutical clinical development principles.Bonus Points:Oncology Therapeutic area experience.Prior PTL experience and attention to detail.What We OfferA competitive salary package.A dynamic and supportive work environment.Opportunities for professional growth and development.About UsWe are a company that values innovation, collaboration and customer satisfaction. We are committed to delivering high-quality solutions that meet our customers' needs.

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