Data Scientist for Clinical Trials

1 week ago

vijayawada, India beBeeStatistical Full time

Job Overview:We are seeking a highly skilled Principal Statistical Programmer to work on clinical development programs across different therapeutic areas.About the Role:This is an exciting opportunity to contribute to our team as a statistical expert, working closely with pharmaceutical clients to drive innovation and empower patients. As a member of our team, you will be responsible for implementing all reporting and analysis activities for clinical trials, developing high-quality statistical programming results, and collaborating with internal and external functions to ensure project timelines and goals are met.Main Responsibilities:Develop SDTM, ADaM specifications, datasets, reviewer's guide, and define.xml files for multiple studies.Create SAS programs to generate datasets, complex listings, tables, and graphs.Deliver high-quality statistical programming results, including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs.Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet pre-specified timelines.Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses.Requirements:Bachelor's degree in Computer Science, Data Science, Mathematics, or Statistics major preferred.7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or similar team and experience supporting drug development, medical device development, or intervention studies.Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment.

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