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Tier-1 brand, Bangalore metro location, and mid-level (5yr) role increase applicant competition.
Clinical SAS and CDISC regulatory expertise makes the role highly industry-specific and less transferable.
Mandatory 5+ years, advanced SAS/CDISC skills and regulatory experience create stringent shortlisting filters.
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Lead and deliver statistical programming activities for clinical study reports, regulatory submissions, and commercialization within Oncology clinical development.
Provide advanced SAS programming expertise and ensure compliance with technical and regulatory standards.
Manage multiple concurrent studies and collaborate globally to support data analysis and reporting processes impacting drug development.
Bachelor's or Master's degree in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field.
Minimum 5 years industry experience in pharmaceutical or healthcare programming with advanced SAS skills.
Strong knowledge of CDISC standards and regulatory programming requirements.
Hybrid work location: Manyata Tech Park, Bangalore with at least 3 days per week onsite.
Experienced leader in statistical programming with prior study lead experience in clinical trials, preferably Oncology therapeutic area.
Ability to influence stakeholders and manage submissions in a global, regulated pharmaceutical environment.
Operates independently on complex programming tasks with a detail-oriented, multitasking approach within cross-functional, international teams.