Clinical SAS Programmer

Found in: Whatjobs IN C2 - 3 weeks ago

bangalore, India Lifelancer Full time

About the job One of our clients is looking for Clinical SAS programmer.This is a remote position.Location: PAN India (WFH)
JOB Description: Graduate/Post-Graduate in Statistics/Mathematics/Computer Science/Life Sciences. At least 7 years of experience in Statistical programming (ADaM)and/or design and analysis of Phase I to Phase IV clinical trials in a Contract Research Organization or Pharmaceutical or Biotechnology Company. Thorough knowledge of the pharmaceutical industry including the understanding of the clinical drug development process and associated documents and regulations. Good knowledge of GCP, Good Programming Practices, ICH-E3, ICH-E9 and other regulatory guidance documents (e.g. USFDA and EMEA) Understanding clients requirement and providing all the required statistical inputs on, SAP, Mock Shells, Tables, Listings, Figures or any other statistical programming deliveries Good understanding of the statistical programming domain and related processes Assists with developing, monitoring, and enforcing productivity and quality standards along with related documentations Coordinating with the project management in meeting the timeline and defining/ capturing the metrics for monitoring and maintaining the quality and productivity Good verbal and written communication skills coupled with good organizational skills
Technical: Strong Analytical and programming Skills using statistical software SAS or equivalent with understanding of development and/or execution of SAS macros Knowledge of R will be an added advantage Should have worked on generating and validating tables, listings and figures Should have worked on Derived datasets/Analysis Datasets/ADaM More complex review (programs with high risk) Programming and review of outputs for DSUR,PSUR, publications Exposure on Exploratory analyses is an added advantage Programming and review of analysis data sets. Provide training and guidance to lower level and new staff. Experience in submission packages (Define.xml, SDRG, ADRG, P21 reports)
Compliance: Adherence to SOPs and GPP Quality and adherence to timelines. Self-motivation and self-learning Achievement orientation Relationship building ability Inclination towards being process driven.

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