Senior Statistical Programmer

Location

Secunderabad | India

Job description

Statistical programmer will responsible for statistical programing for clinical trial studies. Programmer will develop and validate SAS programs for datasets, and outputs (TLFs).Looking for well experienced candidates with strong motive to thrive in analytics in pharma industry. This position is ideal for the people who are looking for career promotions.

programming support in one or more Phase I-III clinical studies. Programming on SDTM and ADaM datasets, including production and validation. Programing tables, listings, figures (TFL), including production and validation. Create SDTM and Adam specifications, or review specifications and provide comments. Prepare e-sub packages for regulatory submissions. Work on ad-hoc requests, medical marketing access presentations, manuscripts and any other requests. Architect and execute utility macros to increase programing efficiency. Mentor junior programmers and guide them with company and client standards. Act as lead programmer for assigned projects, and take responsibility for all programing activities of the study. Foresee the deliverable, commitments and their associated risks, communicate with resourcing manager periodically.

Bachelors degree in Statistics, Biostatistics Mathematics or other science related degree. 5+ years of experience in SAS programing in clinical industry. Complete understanding of clinical trial study designs and statistical analysis. 3+ years of working experience on CDISC standards. Experience in regulatory submission process in at least one clinical trial study. Certification in Base SAS, Clinical SAS and Advanced SAS. Excellent communication and interpersonal skills to effectively interact with others. Team lead experience is added weight.

Job tags

Salary