| Senior Statistical Programming Consultant at Remote, Remote, USA |
| Email: [email protected] |
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From: shrasti singh, vyzeinc [email protected] Reply to: [email protected] Job Description - Senior Statistical Programming Consultant Remote, 12-month contract with potential to renew Qualifications: Bachelors or Masters degree in biostatistics, computer science, or related fields, Masters degree preferred; At least 6 years of relevant experience in the biotech or pharmaceutical industry. The ideal candidate must be able to communicate effectively within a multi-disciplinary project team to assess priorities and complete assigned tasks on time. Proficient of SAS programming in a regulated clinical research environment Experience of programming and validation of SDTM and ADaM data sets, tables, figures, and listings. Responsibilities: Provide statistical programming support to generate SDTM and ADaM datasets, tables, listings, and figures for individual studies and ISS/ISE to FDA, EMA, and other worldwide regulatory agencies Participate in the review of statistical analysis plans and TLF specifications Review or annotate CRFs for SDTM mapping, review/author SDTM/ADaM dataset specifications Review, and comment on CRFs, vendor data transfer specifications (DTS), edit checks and other study data related documents Support in the preparation of study reports, regulatory submissions, and annual safety update reports Perform additional analysis and validation for data checking, publication, presentation, poster and ad hoc analysis Work with CRO statistical programmers and perform statistical programming vendor oversight Contribute to Biometrics SOPs and work instructions related to EDC studies, FDA requests, and statistical programming processes Contribute to department process improvement initiatives Keep abreast of literature and advancements in SAS. Keywords: active directory Senior Statistical Programming Consultant [email protected] |
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| 04:42 AM 12-Mar-25 |