Sr Biostat Programmer Max 95hr W2 Remote

Job Description W2 Candidates only !! Woodcliff Lake NJ, 07677 - This can be 100% remote. Candidates need to work in the EST and must be located in the US. Qualifications and education required: MS in Biostatistics/Statistics preferred, with at least 7 years of experience in the pharmaceutical, CRO, or biotech industry. Strong SAS programming skills, with experience in SAS-Base, MACRO, STAT, and GRAPH. Strong CDISC data standards knowledge, e.g. SDTM and ADaM. Good technical writing skills. Strong verbal, written, and interpersonal communication skills. Strong organizational skills with the ability to effectively manage multiple projects. Strong teamwork ability/commitment and individual initiative. Proven experience with UNIX and Windows operating systems. Understanding of the software development life cycle. Understanding of FDA guidelines. Good organization, time management, and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality. Applies good judgment and demonstrates initiative to resolve issues. Responsibilities: Support the Biostatistics team by carrying out programming activities of statistical programmers and collaborating closely with clinicians, programmers, study teams, and publication managers to generate and QC outputs. Ensure timely and accurate programming and validation activities for clinical studies and publications. Review abstracts/manuscripts (publications) to ensure accuracy, quality, and soundness of statistical methodologies, and oversee external vendors as required. Additionally, oversee CRO programming activities, perform quality assurance checks on internally or externally produced SAS tables, listings, and figures, ensure the quality of CRO deliverables, and work on submission teams as a statistician and/or a programmer. Additional Information: All your information will be kept confidential according to EEO guidelines. #J-18808-Ljbffr

Created: 2025-01-15