Back
Tier-1 brand and Bangalore location increase applicants, but specialized SAS/CDISC skills limit competition.
SAS, CDISC, and regulatory clinical trial experience limit transferability across industries.
Mandatory 4+ years, advanced SAS and CDISC expertise and regulatory experience create strict shortlisting filters.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Provide statistical programming support and/or lead programming activities for clinical study analysis and reporting in oncology projects.
Contribute to clinical study report development, regulatory submissions, commercialization, and scientific data utilization for AstraZeneca products.
Manage multiple concurrent studies with attention to detail within the Oncology Biometrics Programming department.
Bachelor’s or Master’s degree in Mathematics, Statistics, Computer Science, Life or Social Sciences, or related field.
At least 2 years of industry experience with a Master’s degree OR 4+ years with a Bachelor’s degree.
Extensive advanced SAS programming expertise in clinical drug development.
Knowledge of technical and regulatory programming requirements and CDISC standards in clinical trials.
Experience leading study programming activities or trials in clinical settings, preferably oncology.
Ability to work independently and collaboratively within a global team environment on complex programming tasks.
Strong understanding of regulatory and technical standards applied in pharmaceutical programming and drug development.